Canonical Allele Identifier: CA1726776459
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94422975G= , CM000669.2:g.94422975G= GRCh38
NC_000007.13:g.94052287G= , CM000669.1:g.94052287G= GRCh37
NC_000007.12:g.93890223G= NCBI36
NG_007405.1:g.33415G= , LRG_2:g.33415G=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.2422G= MANE Select ENSP00000297268.6:p.Gly808=
ENST00000297268.10:c.2422G= ENSP00000297268.6:p.Gly808=
ENST00000481570.5:n.505G=
ENST00000497316.5:n.819G=
ENST00000620463.1:c.2416G= ENSP00000477719.1:p.Gly806=
NM_000089.3:c.2422G= , LRG_2t1:c.2422G= NP_000080.2:p.Gly808=
NM_000089.4:c.2422G= MANE Select NP_000080.2:p.Gly808=