Canonical Allele Identifier: CA162937903
Gene: COL1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1017681636

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94422884A>G , CM000669.2:g.94422884A>G GRCh38
NC_000007.13:g.94052196A>G , CM000669.1:g.94052196A>G GRCh37
NC_000007.12:g.93890132A>G NCBI36
NG_007405.1:g.33324A>G , LRG_2:g.33324A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.2404-73A>G MANE Select ENSP00000297268.6:n.2404-73A>G
ENST00000297268.10:c.2404-73A>G ENSP00000297268.6:n.2404-73A>G
ENST00000481570.5:n.414A>G
ENST00000497316.5:n.801-73A>G
ENST00000620463.1:c.2398-73A>G ENSP00000477719.1:n.2398-73A>G
NM_000089.3:c.2404-73A>G , LRG_2t1:c.2404-73A>G NP_000080.2:n.2404-73A>G
NM_000089.4:c.2404-73A>G MANE Select NP_000080.2:n.2404-73A>G