Canonical Allele Identifier: CA421942800
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173879045T>C (hg19)

Genomic Alleles

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

Transcript Alleles

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