Canonical Allele Identifier: CA1726776185
Gene: COL1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1792195127

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94422829C>T , CM000669.2:g.94422829C>T GRCh38
NC_000007.13:g.94052141C>T , CM000669.1:g.94052141C>T GRCh37
NC_000007.12:g.93890077C>T NCBI36
NG_007405.1:g.33269C>T , LRG_2:g.33269C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.2404-128C>T MANE Select ENSP00000297268.6:n.2404-128C>T
ENST00000297268.10:c.2404-128C>T ENSP00000297268.6:n.2404-128C>T
ENST00000481570.5:n.359C>T
ENST00000497316.5:n.801-128C>T
ENST00000620463.1:c.2398-128C>T ENSP00000477719.1:n.2398-128C>T
NM_000089.3:c.2404-128C>T , LRG_2t1:c.2404-128C>T NP_000080.2:n.2404-128C>T
NM_000089.4:c.2404-128C>T MANE Select NP_000080.2:n.2404-128C>T