Canonical Allele Identifier: CA162937933
Gene: COL1A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1075257
ClinVar RCV Id: RCV002242851
dbSNP Id: rs72658190

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94422966G>T , CM000669.2:g.94422966G>T GRCh38
NC_000007.13:g.94052278G>T , CM000669.1:g.94052278G>T GRCh37
NC_000007.12:g.93890214G>T NCBI36
NG_007405.1:g.33406G>T , LRG_2:g.33406G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.2413G>T MANE Select ENSP00000297268.6:p.Gly805Cys
ENST00000297268.10:c.2413G>T ENSP00000297268.6:p.Gly805Cys
ENST00000481570.5:n.496G>T
ENST00000497316.5:n.810G>T
ENST00000620463.1:c.2407G>T ENSP00000477719.1:p.Gly803Cys
NM_000089.3:c.2413G>T , LRG_2t1:c.2413G>T NP_000080.2:p.Gly805Cys
NM_000089.4:c.2413G>T MANE Select NP_000080.2:p.Gly805Cys