Canonical Allele Identifier: CA1726776414
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94422958G= , CM000669.2:g.94422958G= GRCh38
NC_000007.13:g.94052270G= , CM000669.1:g.94052270G= GRCh37
NC_000007.12:g.93890206G= NCBI36
NG_007405.1:g.33398G= , LRG_2:g.33398G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.2405G= MANE Select ENSP00000297268.6:p.Gly802=
ENST00000297268.10:c.2405G= ENSP00000297268.6:p.Gly802=
ENST00000481570.5:n.488G=
ENST00000497316.5:n.802G=
ENST00000620463.1:c.2399G= ENSP00000477719.1:p.Gly800=
NM_000089.3:c.2405G= , LRG_2t1:c.2405G= NP_000080.2:p.Gly802=
NM_000089.4:c.2405G= MANE Select NP_000080.2:p.Gly802=