Canonical Allele Identifier: CA1726749570
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94408815G= , CM000669.2:g.94408815G= GRCh38
NC_000007.13:g.94038127G= , CM000669.1:g.94038127G= GRCh37
NC_000007.12:g.93876063G= NCBI36
NG_007405.1:g.19255G= , LRG_2:g.19255G=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.784G= MANE Select ENSP00000297268.6:p.Gly262=
ENST00000297268.10:c.784G= ENSP00000297268.6:p.Gly262=
ENST00000620463.1:c.778G= ENSP00000477719.1:p.Gly260=
NM_000089.3:c.784G= , LRG_2t1:c.784G= NP_000080.2:p.Gly262=
NM_000089.4:c.784G= MANE Select NP_000080.2:p.Gly262=