Canonical Allele Identifier: CA421942936
Gene: SERPINC1 HGNC NCBI

Linked Data

gnomAD v4: 1-173909709-G-T
MyVariant Identifiers: chr1:g.173878847G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909709G>T , CM000663.2:g.173909709G>T GRCh38
NC_000001.10:g.173878847G>T , CM000663.1:g.173878847G>T GRCh37
NC_000001.9:g.172145470G>T NCBI36
NG_012462.1:g.12670C>A , LRG_577:g.12670C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.996C>A MANE Select ENSP00000356671.3:p.Thr332=
ENST00000367698.3:c.996C>A ENSP00000356671.3:p.Thr332=
ENST00000617423.4:c.559+2155C>A ENSP00000478688.1:n.559+2155C>A
NM_000488.3:c.996C>A , LRG_577t1:c.996C>A NP_000479.1:p.Thr332=
XM_005245198.2:c.852C>A XP_005245255.1:p.Thr284=
NM_001365052.1:c.852C>A NP_001351981.1:p.Thr284=
NM_000488.4:c.996C>A MANE Select NP_000479.1:p.Thr332=
NM_001365052.2:c.852C>A NP_001351981.1:p.Thr284=
NM_001386302.1:c.1119C>A NP_001373231.1:p.Thr373=
NM_001386303.1:c.1077C>A NP_001373232.1:p.Thr359=
NM_001386304.1:c.975C>A NP_001373233.1:p.Thr325=
NM_001386305.1:c.939C>A NP_001373234.1:p.Thr313=
NM_001386306.1:c.780C>A NP_001373235.1:p.Thr260=
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