Canonical Allele Identifier: CA101664471

Gene: ADH1C ADH1B

Linked Data

• dbSNP Id: rs747675442
• gnomAD v3: 4-99340922-C-T
• gnomAD v4: 4-99340922-C-T
• MyVariant Identifiers: chr4:g.100262079C>T (hg19) ; chr4:g.99340922C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99340922C>T , CM000666.2:g.99340922C>T	GRCh38
NC_000004.11:g.100262079C>T , CM000666.1:g.100262079C>T	GRCh37
NC_000004.10:g.100481102C>T	NCBI36
NG_011718.1:g.16839G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000515683.6:c.829-212G>A (ADH1C) MANE Select	ENSP00000426083.1:n.829-212G>A
ENST00000639454.1:c.18+11736G>A (ADH1B)	ENSP00000491622.1:n.18+11736G>A
ENST00000515683.5:c.829-212G>A (ADH1C)	ENSP00000426083.1:n.829-212G>A
NM_000669.4:c.829-212G>A (ADH1C)	NP_000660.1:n.829-212G>A
NR_133005.1:n.1155-212G>A (ADH1C)
XM_011531588.1:c.727-212G>A (ADH1C)	XP_011529890.1:n.727-212G>A
XM_011531589.1:c.709-212G>A (ADH1C)	XP_011529891.1:n.709-212G>A
NM_000669.5:c.829-212G>A (ADH1C) MANE Select	NP_000660.1:n.829-212G>A
NR_133005.2:n.856-212G>A (ADH1C)