Canonical Allele Identifier: CA456489643
Gene: COL1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1373660363
gnomAD v4: 7-94423070-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94423070C>A , CM000669.2:g.94423070C>A GRCh38
NC_000007.13:g.94052382C>A , CM000669.1:g.94052382C>A GRCh37
NC_000007.12:g.93890318C>A NCBI36
NG_007405.1:g.33510C>A , LRG_2:g.33510C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.2517C>A MANE Select ENSP00000297268.6:p.Pro839=
ENST00000297268.10:c.2517C>A ENSP00000297268.6:p.Pro839=
ENST00000481570.5:n.600C>A
ENST00000497316.5:n.914C>A
ENST00000620463.1:c.2511C>A ENSP00000477719.1:p.Pro837=
NM_000089.3:c.2517C>A , LRG_2t1:c.2517C>A NP_000080.2:p.Pro839=
NM_000089.4:c.2517C>A MANE Select NP_000080.2:p.Pro839=