Canonical Allele Identifier: CA343774726
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173879037T>C (hg19) chr1:g.173909899T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909899T>C , CM000663.2:g.173909899T>C GRCh38
NC_000001.10:g.173879037T>C , CM000663.1:g.173879037T>C GRCh37
NC_000001.9:g.172145660T>C NCBI36
NG_012462.1:g.12480A>G , LRG_577:g.12480A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.806A>G MANE Select ENSP00000356671.3:p.Glu269Gly
ENST00000367698.3:c.806A>G ENSP00000356671.3:p.Glu269Gly
ENST00000487183.1:n.457A>G
ENST00000617423.4:c.559+1965A>G ENSP00000478688.1:n.559+1965A>G
NM_000488.3:c.806A>G , LRG_577t1:c.806A>G NP_000479.1:p.Glu269Gly
XM_005245198.2:c.662A>G XP_005245255.1:p.Glu221Gly
NM_001365052.1:c.662A>G NP_001351981.1:p.Glu221Gly
NM_000488.4:c.806A>G MANE Select NP_000479.1:p.Glu269Gly
NM_001365052.2:c.662A>G NP_001351981.1:p.Glu221Gly
NM_001386302.1:c.929A>G NP_001373231.1:p.Glu310Gly
NM_001386303.1:c.887A>G NP_001373232.1:p.Glu296Gly
NM_001386304.1:c.785A>G NP_001373233.1:p.Glu262Gly
NM_001386305.1:c.763-14A>G NP_001373234.1:n.763-14A>G
NM_001386306.1:c.590A>G NP_001373235.1:p.Glu197Gly
Search 100 bp 5'
Search 100 bp 3'