Canonical Allele Identifier: CA368223887
Gene: COL1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94422966G>C , CM000669.2:g.94422966G>C GRCh38
NC_000007.13:g.94052278G>C , CM000669.1:g.94052278G>C GRCh37
NC_000007.12:g.93890214G>C NCBI36
NG_007405.1:g.33406G>C , LRG_2:g.33406G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.2413G>C MANE Select ENSP00000297268.6:p.Gly805Arg
ENST00000297268.10:c.2413G>C ENSP00000297268.6:p.Gly805Arg
ENST00000481570.5:n.496G>C
ENST00000497316.5:n.810G>C
ENST00000620463.1:c.2407G>C ENSP00000477719.1:p.Gly803Arg
NM_000089.3:c.2413G>C , LRG_2t1:c.2413G>C NP_000080.2:p.Gly805Arg
NM_000089.4:c.2413G>C MANE Select NP_000080.2:p.Gly805Arg