Canonical Allele Identifier: CA1479960192

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99337040C= , CM000666.2:g.99337040C= GRCh38
NC_000004.11:g.100258197C= , CM000666.1:g.100258197C= GRCh37
NC_000004.10:g.100477220C= NCBI36
NG_011718.1:g.20721G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000515683.6:c.1104-264G= (ADH1C) MANE Select ENSP00000426083.1:n.1104-264G=
ENST00000639454.1:c.18+15618G= (ADH1B) ENSP00000491622.1:n.18+15618G=
ENST00000515683.5:c.1104-264G= (ADH1C) ENSP00000426083.1:n.1104-264G=
NM_000669.4:c.1104-264G= (ADH1C) NP_000660.1:n.1104-264G=
NR_133005.1:n.1430-264G= (ADH1C)
XM_011531588.1:c.1002-264G= (ADH1C) XP_011529890.1:n.1002-264G=
XM_011531589.1:c.984-264G= (ADH1C) XP_011529891.1:n.984-264G=
NM_000669.5:c.1104-264G= (ADH1C) MANE Select NP_000660.1:n.1104-264G=
NR_133005.2:n.1131-264G= (ADH1C)