Canonical Allele Identifier: CA2683773808

Gene: COL1A2

Linked Data

• gnomAD v4: 7-94426587-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.94426587A>G , CM000669.2:g.94426587A>G	GRCh38
NC_000007.13:g.94055899A>G , CM000669.1:g.94055899A>G	GRCh37
NC_000007.12:g.93893835A>G	NCBI36
NG_007405.1:g.37027A>G , LRG_2:g.37027A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297268.11:c.3105+57A>G MANE Select	ENSP00000297268.6:n.3105+57A>G
ENST00000297268.10:c.3105+57A>G	ENSP00000297268.6:n.3105+57A>G
ENST00000478215.1:n.721A>G
ENST00000481570.5:n.3135A>G
ENST00000488121.1:n.21+57A>G
ENST00000620463.1:c.3099+57A>G	ENSP00000477719.1:n.3099+57A>G
NM_000089.3:c.3105+57A>G , LRG_2t1:c.3105+57A>G	NP_000080.2:n.3105+57A>G
NM_000089.4:c.3105+57A>G MANE Select	NP_000080.2:n.3105+57A>G