Canonical Allele Identifier: CA1726776902
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94423080G= , CM000669.2:g.94423080G= GRCh38
NC_000007.13:g.94052392G= , CM000669.1:g.94052392G= GRCh37
NC_000007.12:g.93890328G= NCBI36
NG_007405.1:g.33520G= , LRG_2:g.33520G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.2527G= MANE Select ENSP00000297268.6:p.Ala843=
ENST00000297268.10:c.2527G= ENSP00000297268.6:p.Ala843=
ENST00000481570.5:n.610G=
ENST00000497316.5:n.924G=
ENST00000620463.1:c.2521G= ENSP00000477719.1:p.Ala841=
NM_000089.3:c.2527G= , LRG_2t1:c.2527G= NP_000080.2:p.Ala843=
NM_000089.4:c.2527G= MANE Select NP_000080.2:p.Ala843=