Canonical Allele Identifier: CA2671521823

Gene: ADH1C ADH1B

Linked Data

• gnomAD v4: 4-99336915-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99336915T>G , CM000666.2:g.99336915T>G	GRCh38
NC_000004.11:g.100258072T>G , CM000666.1:g.100258072T>G	GRCh37
NC_000004.10:g.100477095T>G	NCBI36
NG_011718.1:g.20846A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000515683.6:c.1104-139A>C (ADH1C) MANE Select	ENSP00000426083.1:n.1104-139A>C
ENST00000639454.1:c.18+15743A>C (ADH1B)	ENSP00000491622.1:n.18+15743A>C
ENST00000515683.5:c.1104-139A>C (ADH1C)	ENSP00000426083.1:n.1104-139A>C
NM_000669.4:c.1104-139A>C (ADH1C)	NP_000660.1:n.1104-139A>C
NR_133005.1:n.1430-139A>C (ADH1C)
XM_011531588.1:c.1002-139A>C (ADH1C)	XP_011529890.1:n.1002-139A>C
XM_011531589.1:c.984-139A>C (ADH1C)	XP_011529891.1:n.984-139A>C
NM_000669.5:c.1104-139A>C (ADH1C) MANE Select	NP_000660.1:n.1104-139A>C
NR_133005.2:n.1131-139A>C (ADH1C)