Canonical Allele Identifier: CA1726792136
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404558C= , CM000669.2:g.94404558C= GRCh38
NC_000007.13:g.94033870C= , CM000669.1:g.94033870C= GRCh37
NC_000007.12:g.93871806C= NCBI36
NG_007405.1:g.14998C= , LRG_2:g.14998C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.282C= MANE Select ENSP00000297268.6:p.Gly94=
ENST00000297268.10:c.282C= ENSP00000297268.6:p.Gly94=
ENST00000620463.1:c.276C= ENSP00000477719.1:p.Gly92=
NM_000089.3:c.282C= , LRG_2t1:c.282C= NP_000080.2:p.Gly94=
NM_000089.4:c.282C= MANE Select NP_000080.2:p.Gly94=