Canonical Allele Identifier: CA343772066
Gene: SERPINC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 626996
ClinVar RCV Id: RCV000851691
dbSNP Id: rs1572084448
MyVariant Identifiers: chr1:g.173873046G>T (hg19) chr1:g.173903908G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903908G>T , CM000663.2:g.173903908G>T GRCh38
NC_000001.10:g.173873046G>T , CM000663.1:g.173873046G>T GRCh37
NC_000001.9:g.172139669G>T NCBI36
NG_012462.1:g.18471C>A , LRG_577:g.18471C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1376C>A MANE Select ENSP00000356671.3:p.Ala459Asp
ENST00000367698.3:c.1376C>A ENSP00000356671.3:p.Ala459Asp
ENST00000617423.4:c.761C>A ENSP00000478688.1:p.Ala254Asp
NM_000488.3:c.1376C>A , LRG_577t1:c.1376C>A NP_000479.1:p.Ala459Asp
XM_005245198.2:c.1232C>A XP_005245255.1:p.Ala411Asp
NM_001365052.1:c.1232C>A NP_001351981.1:p.Ala411Asp
NM_000488.4:c.1376C>A MANE Select NP_000479.1:p.Ala459Asp
NM_001365052.2:c.1232C>A NP_001351981.1:p.Ala411Asp
NM_001386302.1:c.1499C>A NP_001373231.1:p.Ala500Asp
NM_001386303.1:c.1457C>A NP_001373232.1:p.Ala486Asp
NM_001386304.1:c.1355C>A NP_001373233.1:p.Ala452Asp
NM_001386305.1:c.1319C>A NP_001373234.1:p.Ala440Asp
NM_001386306.1:c.1160C>A NP_001373235.1:p.Ala387Asp
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