Canonical Allele Identifier: CA343772398
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173873112T>G (hg19) chr1:g.173903974T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903974T>G , CM000663.2:g.173903974T>G GRCh38
NC_000001.10:g.173873112T>G , CM000663.1:g.173873112T>G GRCh37
NC_000001.9:g.172139735T>G NCBI36
NG_012462.1:g.18405A>C , LRG_577:g.18405A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1310A>C MANE Select ENSP00000356671.3:p.Asn437Thr
ENST00000367698.3:c.1310A>C ENSP00000356671.3:p.Asn437Thr
ENST00000617423.4:c.695A>C ENSP00000478688.1:p.Asn232Thr
NM_000488.3:c.1310A>C , LRG_577t1:c.1310A>C NP_000479.1:p.Asn437Thr
XM_005245198.2:c.1166A>C XP_005245255.1:p.Asn389Thr
NM_001365052.1:c.1166A>C NP_001351981.1:p.Asn389Thr
NM_000488.4:c.1310A>C MANE Select NP_000479.1:p.Asn437Thr
NM_001365052.2:c.1166A>C NP_001351981.1:p.Asn389Thr
NM_001386302.1:c.1433A>C NP_001373231.1:p.Asn478Thr
NM_001386303.1:c.1391A>C NP_001373232.1:p.Asn464Thr
NM_001386304.1:c.1289A>C NP_001373233.1:p.Asn430Thr
NM_001386305.1:c.1253A>C NP_001373234.1:p.Asn418Thr
NM_001386306.1:c.1094A>C NP_001373235.1:p.Asn365Thr
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