Canonical Allele Identifier: CA1726776279
Gene: COL1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1792196442

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94422895T>C , CM000669.2:g.94422895T>C GRCh38
NC_000007.13:g.94052207T>C , CM000669.1:g.94052207T>C GRCh37
NC_000007.12:g.93890143T>C NCBI36
NG_007405.1:g.33335T>C , LRG_2:g.33335T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.2404-62T>C MANE Select ENSP00000297268.6:n.2404-62T>C
ENST00000297268.10:c.2404-62T>C ENSP00000297268.6:n.2404-62T>C
ENST00000481570.5:n.425T>C
ENST00000497316.5:n.801-62T>C
ENST00000620463.1:c.2398-62T>C ENSP00000477719.1:n.2398-62T>C
NM_000089.3:c.2404-62T>C , LRG_2t1:c.2404-62T>C NP_000080.2:n.2404-62T>C
NM_000089.4:c.2404-62T>C MANE Select NP_000080.2:n.2404-62T>C