Canonical Allele Identifier: CA101664478

Gene: ADH1C ADH1B

Linked Data

• dbSNP Id: rs995596096
• MyVariant Identifiers: chr4:g.100262080G>A (hg19) ; chr4:g.99340923G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99340923G>A , CM000666.2:g.99340923G>A	GRCh38
NC_000004.11:g.100262080G>A , CM000666.1:g.100262080G>A	GRCh37
NC_000004.10:g.100481103G>A	NCBI36
NG_011718.1:g.16838C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000515683.6:c.829-213C>T (ADH1C) MANE Select	ENSP00000426083.1:n.829-213C>T
ENST00000639454.1:c.18+11735C>T (ADH1B)	ENSP00000491622.1:n.18+11735C>T
ENST00000515683.5:c.829-213C>T (ADH1C)	ENSP00000426083.1:n.829-213C>T
NM_000669.4:c.829-213C>T (ADH1C)	NP_000660.1:n.829-213C>T
NR_133005.1:n.1155-213C>T (ADH1C)
XM_011531588.1:c.727-213C>T (ADH1C)	XP_011529890.1:n.727-213C>T
XM_011531589.1:c.709-213C>T (ADH1C)	XP_011529891.1:n.709-213C>T
NM_000669.5:c.829-213C>T (ADH1C) MANE Select	NP_000660.1:n.829-213C>T
NR_133005.2:n.856-213C>T (ADH1C)