Canonical Allele Identifier: CA343774662
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs1572088795
MyVariant Identifiers: chr1:g.173879022G>A (hg19) chr1:g.173909884G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909884G>A , CM000663.2:g.173909884G>A GRCh38
NC_000001.10:g.173879022G>A , CM000663.1:g.173879022G>A GRCh37
NC_000001.9:g.172145645G>A NCBI36
NG_012462.1:g.12495C>T , LRG_577:g.12495C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.821C>T MANE Select ENSP00000356671.3:p.Ala274Val
ENST00000367698.3:c.821C>T ENSP00000356671.3:p.Ala274Val
ENST00000487183.1:n.472C>T
ENST00000617423.4:c.559+1980C>T ENSP00000478688.1:n.559+1980C>T
NM_000488.3:c.821C>T , LRG_577t1:c.821C>T NP_000479.1:p.Ala274Val
XM_005245198.2:c.677C>T XP_005245255.1:p.Ala226Val
NM_001365052.1:c.677C>T NP_001351981.1:p.Ala226Val
NM_000488.4:c.821C>T MANE Select NP_000479.1:p.Ala274Val
NM_001365052.2:c.677C>T NP_001351981.1:p.Ala226Val
NM_001386302.1:c.944C>T NP_001373231.1:p.Ala315Val
NM_001386303.1:c.902C>T NP_001373232.1:p.Ala301Val
NM_001386304.1:c.800C>T NP_001373233.1:p.Ala267Val
NM_001386305.1:c.764C>T NP_001373234.1:p.Ala255Val
NM_001386306.1:c.605C>T NP_001373235.1:p.Ala202Val
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