Canonical Allele Identifier: CA527601324
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs1398790792
gnomAD v2: 1-173873347-G-A
gnomAD v3: 1-173904209-G-A
gnomAD v4: 1-173904209-G-A
MyVariant Identifiers: chr1:g.173873347G>A (hg19) chr1:g.173904209G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173904209G>A , CM000663.2:g.173904209G>A GRCh38
NC_000001.10:g.173873347G>A , CM000663.1:g.173873347G>A GRCh37
NC_000001.9:g.172139970G>A NCBI36
NG_012462.1:g.18170C>T , LRG_577:g.18170C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1219-144C>T MANE Select ENSP00000356671.3:n.1219-144C>T
ENST00000367698.3:c.1219-144C>T ENSP00000356671.3:n.1219-144C>T
ENST00000617423.4:c.604-144C>T ENSP00000478688.1:n.604-144C>T
NM_000488.3:c.1219-144C>T , LRG_577t1:c.1219-144C>T NP_000479.1:n.1219-144C>T
XM_005245198.2:c.1075-144C>T XP_005245255.1:n.1075-144C>T
NM_001365052.1:c.1075-144C>T NP_001351981.1:n.1075-144C>T
NM_000488.4:c.1219-144C>T MANE Select NP_000479.1:n.1219-144C>T
NM_001365052.2:c.1075-144C>T NP_001351981.1:n.1075-144C>T
NM_001386302.1:c.1342-144C>T NP_001373231.1:n.1342-144C>T
NM_001386303.1:c.1300-144C>T NP_001373232.1:n.1300-144C>T
NM_001386304.1:c.1198-144C>T NP_001373233.1:n.1198-144C>T
NM_001386305.1:c.1162-144C>T NP_001373234.1:n.1162-144C>T
NM_001386306.1:c.1003-144C>T NP_001373235.1:n.1003-144C>T
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