Canonical Allele Identifier: CA1479962114

Gene: ADH1C ADH1B

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99340931T= , CM000666.2:g.99340931T=	GRCh38
NC_000004.11:g.100262088T= , CM000666.1:g.100262088T=	GRCh37
NC_000004.10:g.100481111T=	NCBI36
NG_011718.1:g.16830A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000515683.6:c.829-221A= (ADH1C) MANE Select	ENSP00000426083.1:n.829-221A=
ENST00000639454.1:c.18+11727A= (ADH1B)	ENSP00000491622.1:n.18+11727A=
ENST00000515683.5:c.829-221A= (ADH1C)	ENSP00000426083.1:n.829-221A=
NM_000669.4:c.829-221A= (ADH1C)	NP_000660.1:n.829-221A=
NR_133005.1:n.1155-221A= (ADH1C)
XM_011531588.1:c.727-221A= (ADH1C)	XP_011529890.1:n.727-221A=
XM_011531589.1:c.709-221A= (ADH1C)	XP_011529891.1:n.709-221A=
NM_000669.5:c.829-221A= (ADH1C) MANE Select	NP_000660.1:n.829-221A=
NR_133005.2:n.856-221A= (ADH1C)