Canonical Allele Identifier: CA1479960166

Gene: ADH1C ADH1B

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99336998C= , CM000666.2:g.99336998C=	GRCh38
NC_000004.11:g.100258155C= , CM000666.1:g.100258155C=	GRCh37
NC_000004.10:g.100477178C=	NCBI36
NG_011718.1:g.20763G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000515683.6:c.1104-222G= (ADH1C) MANE Select	ENSP00000426083.1:n.1104-222G=
ENST00000639454.1:c.18+15660G= (ADH1B)	ENSP00000491622.1:n.18+15660G=
ENST00000515683.5:c.1104-222G= (ADH1C)	ENSP00000426083.1:n.1104-222G=
NM_000669.4:c.1104-222G= (ADH1C)	NP_000660.1:n.1104-222G=
NR_133005.1:n.1430-222G= (ADH1C)
XM_011531588.1:c.1002-222G= (ADH1C)	XP_011529890.1:n.1002-222G=
XM_011531589.1:c.984-222G= (ADH1C)	XP_011529891.1:n.984-222G=
NM_000669.5:c.1104-222G= (ADH1C) MANE Select	NP_000660.1:n.1104-222G=
NR_133005.2:n.1131-222G= (ADH1C)