Canonical Allele Identifier: CA368222956
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94417824G>A , CM000669.2:g.94417824G>A GRCh38
NC_000007.13:g.94047136G>A , CM000669.1:g.94047136G>A GRCh37
NC_000007.12:g.93885072G>A NCBI36
NG_007405.1:g.28264G>A , LRG_2:g.28264G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.1964G>A MANE Select ENSP00000297268.6:p.Gly655Glu
ENST00000297268.10:c.1964G>A ENSP00000297268.6:p.Gly655Glu
ENST00000461525.5:n.53G>A
ENST00000473573.5:n.301G>A
ENST00000497316.5:n.361G>A
ENST00000620463.1:c.1958G>A ENSP00000477719.1:p.Gly653Glu
NM_000089.3:c.1964G>A , LRG_2t1:c.1964G>A NP_000080.2:p.Gly655Glu
NM_000089.4:c.1964G>A MANE Select NP_000080.2:p.Gly655Glu