Canonical Allele Identifier: CA1726777258
Gene: COL1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1792206558

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94423260C>T , CM000669.2:g.94423260C>T GRCh38
NC_000007.13:g.94052572C>T , CM000669.1:g.94052572C>T GRCh37
NC_000007.12:g.93890508C>T NCBI36
NG_007405.1:g.33700C>T , LRG_2:g.33700C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.2565+142C>T MANE Select ENSP00000297268.6:n.2565+142C>T
ENST00000297268.10:c.2565+142C>T ENSP00000297268.6:n.2565+142C>T
ENST00000481570.5:n.790C>T
ENST00000620463.1:c.2559+142C>T ENSP00000477719.1:n.2559+142C>T
NM_000089.3:c.2565+142C>T , LRG_2t1:c.2565+142C>T NP_000080.2:n.2565+142C>T
NM_000089.4:c.2565+142C>T MANE Select NP_000080.2:n.2565+142C>T