Canonical Allele Identifier: CA2715039003
Gene: COL1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1792196172

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94422866G>A , CM000669.2:g.94422866G>A GRCh38
NC_000007.13:g.94052178G>A , CM000669.1:g.94052178G>A GRCh37
NC_000007.12:g.93890114G>A NCBI36
NG_007405.1:g.33306G>A , LRG_2:g.33306G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.2404-91G>A MANE Select ENSP00000297268.6:n.2404-91G>A
ENST00000297268.10:c.2404-91G>A ENSP00000297268.6:n.2404-91G>A
ENST00000481570.5:n.396G>A
ENST00000497316.5:n.801-91G>A
ENST00000620463.1:c.2398-91G>A ENSP00000477719.1:n.2398-91G>A
NM_000089.3:c.2404-91G>A , LRG_2t1:c.2404-91G>A NP_000080.2:n.2404-91G>A
NM_000089.4:c.2404-91G>A MANE Select NP_000080.2:n.2404-91G>A