Canonical Allele Identifier: CA368223888
Gene: COL1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94422967G>C , CM000669.2:g.94422967G>C GRCh38
NC_000007.13:g.94052279G>C , CM000669.1:g.94052279G>C GRCh37
NC_000007.12:g.93890215G>C NCBI36
NG_007405.1:g.33407G>C , LRG_2:g.33407G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.2414G>C MANE Select ENSP00000297268.6:p.Gly805Ala
ENST00000297268.10:c.2414G>C ENSP00000297268.6:p.Gly805Ala
ENST00000481570.5:n.497G>C
ENST00000497316.5:n.811G>C
ENST00000620463.1:c.2408G>C ENSP00000477719.1:p.Gly803Ala
NM_000089.3:c.2414G>C , LRG_2t1:c.2414G>C NP_000080.2:p.Gly805Ala
NM_000089.4:c.2414G>C MANE Select NP_000080.2:p.Gly805Ala