Canonical Allele Identifier: CA1726792137
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404561A= , CM000669.2:g.94404561A= GRCh38
NC_000007.13:g.94033873A= , CM000669.1:g.94033873A= GRCh37
NC_000007.12:g.93871809A= NCBI36
NG_007405.1:g.15001A= , LRG_2:g.15001A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.285A= MANE Select ENSP00000297268.6:p.Leu95=
ENST00000297268.10:c.285A= ENSP00000297268.6:p.Leu95=
ENST00000620463.1:c.279A= ENSP00000477719.1:p.Leu93=
NM_000089.3:c.285A= , LRG_2t1:c.285A= NP_000080.2:p.Leu95=
NM_000089.4:c.285A= MANE Select NP_000080.2:p.Leu95=