Canonical Allele Identifier: CA357494721

Gene: ADH1C ADH1B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99347033C>T , CM000666.2:g.99347033C>T	GRCh38
NG_011718.1:g.10728G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000515683.6:c.232G>A (ADH1C) MANE Select	ENSP00000426083.1:p.Gly78Arg
ENST00000639454.1:c.18+5625G>A (ADH1B)	ENSP00000491622.1:n.18+5625G>A
ENST00000505942.2:n.301G>A (ADH1C)
ENST00000510055.5:c.112G>A (ADH1C)	ENSP00000478439.1:p.Gly38Arg
ENST00000511397.3:c.130G>A (ADH1C)	ENSP00000478545.1:p.Gly44Arg
ENST00000515683.5:c.232G>A (ADH1C)	ENSP00000426083.1:p.Gly78Arg
NM_000669.4:c.232G>A (ADH1C)	NP_000660.1:p.Gly78Arg
NR_133005.1:n.602G>A (ADH1C)
XM_011531588.1:c.130G>A (ADH1C)	XP_011529890.1:p.Gly44Arg
XM_011531589.1:c.112G>A (ADH1C)	XP_011529891.1:p.Gly38Arg
NM_000669.5:c.232G>A (ADH1C) MANE Select	NP_000660.1:p.Gly78Arg
NR_133005.2:n.303G>A (ADH1C)