Canonical Allele Identifier: CA1726776932
Gene: COL1A2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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