Canonical Allele Identifier: CA16042602
Gene: COL1A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 372734
ClinVar RCV Id: RCV001861415
dbSNP Id: rs1057517953

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94406295G>T , CM000669.2:g.94406295G>T GRCh38
NC_000007.13:g.94035607G>T , CM000669.1:g.94035607G>T GRCh37
NC_000007.12:g.93873543G>T NCBI36
NG_007405.1:g.16735G>T , LRG_2:g.16735G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.586G>T MANE Select ENSP00000297268.6:p.Gly196Cys
ENST00000297268.10:c.586G>T ENSP00000297268.6:p.Gly196Cys
ENST00000620463.1:c.580G>T ENSP00000477719.1:p.Gly194Cys
NM_000089.3:c.586G>T , LRG_2t1:c.586G>T NP_000080.2:p.Gly196Cys
NM_000089.4:c.586G>T MANE Select NP_000080.2:p.Gly196Cys