Canonical Allele Identifier: CA527601260
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs1469720038
gnomAD v2: 1-173878647-A-G
gnomAD v3: 1-173909509-A-G
gnomAD v4: 1-173909509-A-G
MyVariant Identifiers: chr1:g.173878647A>G (hg19) chr1:g.173909509A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909509A>G , CM000663.2:g.173909509A>G GRCh38
NC_000001.10:g.173878647A>G , CM000663.1:g.173878647A>G GRCh37
NC_000001.9:g.172145270A>G NCBI36
NG_012462.1:g.12870T>C , LRG_577:g.12870T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1153+43T>C MANE Select ENSP00000356671.3:n.1153+43T>C
ENST00000367698.3:c.1153+43T>C ENSP00000356671.3:n.1153+43T>C
ENST00000617423.4:c.560-2016T>C ENSP00000478688.1:n.560-2016T>C
NM_000488.3:c.1153+43T>C , LRG_577t1:c.1153+43T>C NP_000479.1:n.1153+43T>C
XM_005245198.2:c.1009+43T>C XP_005245255.1:n.1009+43T>C
NM_001365052.1:c.1009+43T>C NP_001351981.1:n.1009+43T>C
NM_000488.4:c.1153+43T>C MANE Select NP_000479.1:n.1153+43T>C
NM_001365052.2:c.1009+43T>C NP_001351981.1:n.1009+43T>C
NM_001386302.1:c.1276+43T>C NP_001373231.1:n.1276+43T>C
NM_001386303.1:c.1234+43T>C NP_001373232.1:n.1234+43T>C
NM_001386304.1:c.1132+43T>C NP_001373233.1:n.1132+43T>C
NM_001386305.1:c.1096+43T>C NP_001373234.1:n.1096+43T>C
NM_001386306.1:c.937+43T>C NP_001373235.1:n.937+43T>C
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