Canonical Allele Identifier: CA1479960173

Linked Data

dbSNP Id: rs1026215091

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99337007C>T , CM000666.2:g.99337007C>T GRCh38
NC_000004.11:g.100258164C>T , CM000666.1:g.100258164C>T GRCh37
NC_000004.10:g.100477187C>T NCBI36
NG_011718.1:g.20754G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000515683.6:c.1104-231G>A (ADH1C) MANE Select ENSP00000426083.1:n.1104-231G>A
ENST00000639454.1:c.18+15651G>A (ADH1B) ENSP00000491622.1:n.18+15651G>A
ENST00000515683.5:c.1104-231G>A (ADH1C) ENSP00000426083.1:n.1104-231G>A
NM_000669.4:c.1104-231G>A (ADH1C) NP_000660.1:n.1104-231G>A
NR_133005.1:n.1430-231G>A (ADH1C)
XM_011531588.1:c.1002-231G>A (ADH1C) XP_011529890.1:n.1002-231G>A
XM_011531589.1:c.984-231G>A (ADH1C) XP_011529891.1:n.984-231G>A
NM_000669.5:c.1104-231G>A (ADH1C) MANE Select NP_000660.1:n.1104-231G>A
NR_133005.2:n.1131-231G>A (ADH1C)