Canonical Allele Identifier: CA343772520
Gene: SERPINC1 HGNC NCBI

Linked Data

gnomAD v4: 1-173903996-T-C
MyVariant Identifiers: chr1:g.173873134T>C (hg19) chr1:g.173903996T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903996T>C , CM000663.2:g.173903996T>C GRCh38
NC_000001.10:g.173873134T>C , CM000663.1:g.173873134T>C GRCh37
NC_000001.9:g.172139757T>C NCBI36
NG_012462.1:g.18383A>G , LRG_577:g.18383A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1288A>G MANE Select ENSP00000356671.3:p.Asn430Asp
ENST00000367698.3:c.1288A>G ENSP00000356671.3:p.Asn430Asp
ENST00000617423.4:c.673A>G ENSP00000478688.1:p.Asn225Asp
NM_000488.3:c.1288A>G , LRG_577t1:c.1288A>G NP_000479.1:p.Asn430Asp
XM_005245198.2:c.1144A>G XP_005245255.1:p.Asn382Asp
NM_001365052.1:c.1144A>G NP_001351981.1:p.Asn382Asp
NM_000488.4:c.1288A>G MANE Select NP_000479.1:p.Asn430Asp
NM_001365052.2:c.1144A>G NP_001351981.1:p.Asn382Asp
NM_001386302.1:c.1411A>G NP_001373231.1:p.Asn471Asp
NM_001386303.1:c.1369A>G NP_001373232.1:p.Asn457Asp
NM_001386304.1:c.1267A>G NP_001373233.1:p.Asn423Asp
NM_001386305.1:c.1231A>G NP_001373234.1:p.Asn411Asp
NM_001386306.1:c.1072A>G NP_001373235.1:p.Asn358Asp
Search 100 bp 5'
Search 100 bp 3'