Canonical Allele Identifier: CA421942799
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173879045T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909907T>A , CM000663.2:g.173909907T>A GRCh38
NC_000001.10:g.173879045T>A , CM000663.1:g.173879045T>A GRCh37
NC_000001.9:g.172145668T>A NCBI36
NG_012462.1:g.12472A>T , LRG_577:g.12472A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.798A>T MANE Select ENSP00000356671.3:p.Thr266=
ENST00000367698.3:c.798A>T ENSP00000356671.3:p.Thr266=
ENST00000487183.1:n.449A>T
ENST00000617423.4:c.559+1957A>T ENSP00000478688.1:n.559+1957A>T
NM_000488.3:c.798A>T , LRG_577t1:c.798A>T NP_000479.1:p.Thr266=
XM_005245198.2:c.654A>T XP_005245255.1:p.Thr218=
NM_001365052.1:c.654A>T NP_001351981.1:p.Thr218=
NM_000488.4:c.798A>T MANE Select NP_000479.1:p.Thr266=
NM_001365052.2:c.654A>T NP_001351981.1:p.Thr218=
NM_001386302.1:c.921A>T NP_001373231.1:p.Thr307=
NM_001386303.1:c.879A>T NP_001373232.1:p.Thr293=
NM_001386304.1:c.777A>T NP_001373233.1:p.Thr259=
NM_001386305.1:c.763-22A>T NP_001373234.1:n.763-22A>T
NM_001386306.1:c.582A>T NP_001373235.1:p.Thr194=
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