Canonical Allele Identifier: CA1104592855
Gene: COL1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1791865632
gnomAD v3: 7-94409230-A-G
gnomAD v4: 7-94409230-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94409230A>G , CM000669.2:g.94409230A>G GRCh38
NC_000007.13:g.94038542A>G , CM000669.1:g.94038542A>G GRCh37
NC_000007.12:g.93876478A>G NCBI36
NG_007405.1:g.19670A>G , LRG_2:g.19670A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.793-92A>G MANE Select ENSP00000297268.6:n.793-92A>G
ENST00000297268.10:c.793-92A>G ENSP00000297268.6:n.793-92A>G
ENST00000620463.1:c.787-92A>G ENSP00000477719.1:n.787-92A>G
NM_000089.3:c.793-92A>G , LRG_2t1:c.793-92A>G NP_000080.2:n.793-92A>G
NM_000089.4:c.793-92A>G MANE Select NP_000080.2:n.793-92A>G