Canonical Allele Identifier: CA1726777126
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94423169A= , CM000669.2:g.94423169A= GRCh38
NC_000007.13:g.94052481A= , CM000669.1:g.94052481A= GRCh37
NC_000007.12:g.93890417A= NCBI36
NG_007405.1:g.33609A= , LRG_2:g.33609A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.2565+51A= MANE Select ENSP00000297268.6:n.2565+51A=
ENST00000297268.10:c.2565+51A= ENSP00000297268.6:n.2565+51A=
ENST00000481570.5:n.699A=
ENST00000620463.1:c.2559+51A= ENSP00000477719.1:n.2559+51A=
NM_000089.3:c.2565+51A= , LRG_2t1:c.2565+51A= NP_000080.2:n.2565+51A=
NM_000089.4:c.2565+51A= MANE Select NP_000080.2:n.2565+51A=