Canonical Allele Identifier: CA456489654
Gene: COL1A2 HGNC NCBI

Linked Data

gnomAD v4: 7-94423085-T-A
MyVariant Identifiers: chr7:g.94052397T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94423085T>A , CM000669.2:g.94423085T>A GRCh38
NC_000007.13:g.94052397T>A , CM000669.1:g.94052397T>A GRCh37
NC_000007.12:g.93890333T>A NCBI36
NG_007405.1:g.33525T>A , LRG_2:g.33525T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.2532T>A MANE Select ENSP00000297268.6:p.Gly844=
ENST00000297268.10:c.2532T>A ENSP00000297268.6:p.Gly844=
ENST00000481570.5:n.615T>A
ENST00000497316.5:n.929T>A
ENST00000620463.1:c.2526T>A ENSP00000477719.1:p.Gly842=
NM_000089.3:c.2532T>A , LRG_2t1:c.2532T>A NP_000080.2:p.Gly844=
NM_000089.4:c.2532T>A MANE Select NP_000080.2:p.Gly844=