Canonical Allele Identifier: CA1479962996

Gene: ADH1C ADH1B

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99342812C= , CM000666.2:g.99342812C=	GRCh38
NC_000004.11:g.100263969C= , CM000666.1:g.100263969C=	GRCh37
NC_000004.10:g.100482992C=	NCBI36
NG_011718.1:g.14949G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000515683.6:c.811G= (ADH1C) MANE Select	ENSP00000426083.1:p.Gly271=
ENST00000639454.1:c.18+9846G= (ADH1B)	ENSP00000491622.1:n.18+9846G=
ENST00000515683.5:c.811G= (ADH1C)	ENSP00000426083.1:p.Gly271=
NM_000669.4:c.811G= (ADH1C)	NP_000660.1:p.Gly271=
NR_133005.1:n.1154+27G= (ADH1C)
XM_011531588.1:c.709G= (ADH1C)	XP_011529890.1:p.Gly237=
XM_011531589.1:c.691G= (ADH1C)	XP_011529891.1:p.Gly231=
NM_000669.5:c.811G= (ADH1C) MANE Select	NP_000660.1:p.Gly271=
NR_133005.2:n.855+27G= (ADH1C)