Canonical Allele Identifier: CA1104592847
Gene: COL1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1791865365

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94409211A>C , CM000669.2:g.94409211A>C GRCh38
NC_000007.13:g.94038523A>C , CM000669.1:g.94038523A>C GRCh37
NC_000007.12:g.93876459A>C NCBI36
NG_007405.1:g.19651A>C , LRG_2:g.19651A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.793-111A>C MANE Select ENSP00000297268.6:n.793-111A>C
ENST00000297268.10:c.793-111A>C ENSP00000297268.6:n.793-111A>C
ENST00000620463.1:c.787-111A>C ENSP00000477719.1:n.787-111A>C
NM_000089.3:c.793-111A>C , LRG_2t1:c.793-111A>C NP_000080.2:n.793-111A>C
NM_000089.4:c.793-111A>C MANE Select NP_000080.2:n.793-111A>C