Canonical Allele Identifier: CA2536832629
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404799A>G , CM000669.2:g.94404799A>G GRCh38
NC_000007.13:g.94034111A>G , CM000669.1:g.94034111A>G GRCh37
NC_000007.12:g.93872047A>G NCBI36
NG_007405.1:g.15239A>G , LRG_2:g.15239A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.379-40A>G MANE Select ENSP00000297268.6:n.379-40A>G
ENST00000297268.10:c.379-40A>G ENSP00000297268.6:n.379-40A>G
ENST00000620463.1:c.373-40A>G ENSP00000477719.1:n.373-40A>G
NM_000089.3:c.379-40A>G , LRG_2t1:c.379-40A>G NP_000080.2:n.379-40A>G
NM_000089.4:c.379-40A>G MANE Select NP_000080.2:n.379-40A>G