Canonical Allele Identifier: CA1726776877
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94423074G= , CM000669.2:g.94423074G= GRCh38
NC_000007.13:g.94052386G= , CM000669.1:g.94052386G= GRCh37
NC_000007.12:g.93890322G= NCBI36
NG_007405.1:g.33514G= , LRG_2:g.33514G=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.2521G= MANE Select ENSP00000297268.6:p.Gly841=
ENST00000297268.10:c.2521G= ENSP00000297268.6:p.Gly841=
ENST00000481570.5:n.604G=
ENST00000497316.5:n.918G=
ENST00000620463.1:c.2515G= ENSP00000477719.1:p.Gly839=
NM_000089.3:c.2521G= , LRG_2t1:c.2521G= NP_000080.2:p.Gly841=
NM_000089.4:c.2521G= MANE Select NP_000080.2:p.Gly841=