Canonical Allele Identifier: CA2715123841
Gene: COL1A2 HGNC NCBI

Linked Data

dbSNP Id: rs2115863955

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94401272G>A , CM000669.2:g.94401272G>A GRCh38
NC_000007.13:g.94030584G>A , CM000669.1:g.94030584G>A GRCh37
NC_000007.12:g.93868520G>A NCBI36
NG_007405.1:g.11712G>A , LRG_2:g.11712G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.226-295G>A MANE Select ENSP00000297268.6:n.226-295G>A
ENST00000297268.10:c.226-295G>A ENSP00000297268.6:n.226-295G>A
ENST00000620463.1:c.220-295G>A ENSP00000477719.1:n.220-295G>A
NM_000089.3:c.226-295G>A , LRG_2t1:c.226-295G>A NP_000080.2:n.226-295G>A
NM_000089.4:c.226-295G>A MANE Select NP_000080.2:n.226-295G>A