Canonical Allele Identifier: CA800713871

Gene: ADH1C ADH1B

Linked Data

• dbSNP Id: rs1463527872
• gnomAD v3: 4-99337035-A-G
• gnomAD v4: 4-99337035-A-G
• MyVariant Identifiers: chr4:g.100258192A>G (hg19) ; chr4:g.99337035A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99337035A>G , CM000666.2:g.99337035A>G	GRCh38
NC_000004.11:g.100258192A>G , CM000666.1:g.100258192A>G	GRCh37
NC_000004.10:g.100477215A>G	NCBI36
NG_011718.1:g.20726T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000515683.6:c.1104-259T>C (ADH1C) MANE Select	ENSP00000426083.1:n.1104-259T>C
ENST00000639454.1:c.18+15623T>C (ADH1B)	ENSP00000491622.1:n.18+15623T>C
ENST00000515683.5:c.1104-259T>C (ADH1C)	ENSP00000426083.1:n.1104-259T>C
NM_000669.4:c.1104-259T>C (ADH1C)	NP_000660.1:n.1104-259T>C
NR_133005.1:n.1430-259T>C (ADH1C)
XM_011531588.1:c.1002-259T>C (ADH1C)	XP_011529890.1:n.1002-259T>C
XM_011531589.1:c.984-259T>C (ADH1C)	XP_011529891.1:n.984-259T>C
NM_000669.5:c.1104-259T>C (ADH1C) MANE Select	NP_000660.1:n.1104-259T>C
NR_133005.2:n.1131-259T>C (ADH1C)