Canonical Allele Identifier: CA1726776173
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94422824T= , CM000669.2:g.94422824T= GRCh38
NC_000007.13:g.94052136T= , CM000669.1:g.94052136T= GRCh37
NC_000007.12:g.93890072T= NCBI36
NG_007405.1:g.33264T= , LRG_2:g.33264T=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.2404-133T= MANE Select ENSP00000297268.6:n.2404-133T=
ENST00000297268.10:c.2404-133T= ENSP00000297268.6:n.2404-133T=
ENST00000481570.5:n.354T=
ENST00000497316.5:n.801-133T=
ENST00000620463.1:c.2398-133T= ENSP00000477719.1:n.2398-133T=
NM_000089.3:c.2404-133T= , LRG_2t1:c.2404-133T= NP_000080.2:n.2404-133T=
NM_000089.4:c.2404-133T= MANE Select NP_000080.2:n.2404-133T=