Canonical Allele Identifier: CA553103435

Gene: ADH1C ADH1B

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99344800C>T , CM000666.2:g.99344800C>T	GRCh38
NC_000004.11:g.100265957C>T , CM000666.1:g.100265957C>T	GRCh37
NC_000004.10:g.100484980C>T	NCBI36
NG_011718.1:g.12961G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000515683.6:c.567+62G>A (ADH1C) MANE Select	ENSP00000426083.1:n.567+62G>A
ENST00000639454.1:c.18+7858G>A (ADH1B)	ENSP00000491622.1:n.18+7858G>A
ENST00000510055.5:c.447+62G>A (ADH1C)	ENSP00000478439.1:n.447+62G>A
ENST00000511397.3:c.465+62G>A (ADH1C)	ENSP00000478545.1:n.465+62G>A
ENST00000515683.5:c.567+62G>A (ADH1C)	ENSP00000426083.1:n.567+62G>A
NM_000669.4:c.567+62G>A (ADH1C)	NP_000660.1:n.567+62G>A
NR_133005.1:n.937+62G>A (ADH1C)
XM_011531588.1:c.465+62G>A (ADH1C)	XP_011529890.1:n.465+62G>A
XM_011531589.1:c.447+62G>A (ADH1C)	XP_011529891.1:n.447+62G>A
NM_000669.5:c.567+62G>A (ADH1C) MANE Select	NP_000660.1:n.567+62G>A
NR_133005.2:n.638+62G>A (ADH1C)