Canonical Allele Identifier: CA1479962118

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99340938C= , CM000666.2:g.99340938C= GRCh38
NC_000004.11:g.100262095C= , CM000666.1:g.100262095C= GRCh37
NC_000004.10:g.100481118C= NCBI36
NG_011718.1:g.16823G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000515683.6:c.829-228G= (ADH1C) MANE Select ENSP00000426083.1:n.829-228G=
ENST00000639454.1:c.18+11720G= (ADH1B) ENSP00000491622.1:n.18+11720G=
ENST00000515683.5:c.829-228G= (ADH1C) ENSP00000426083.1:n.829-228G=
NM_000669.4:c.829-228G= (ADH1C) NP_000660.1:n.829-228G=
NR_133005.1:n.1155-228G= (ADH1C)
XM_011531588.1:c.727-228G= (ADH1C) XP_011529890.1:n.727-228G=
XM_011531589.1:c.709-228G= (ADH1C) XP_011529891.1:n.709-228G=
NM_000669.5:c.829-228G= (ADH1C) MANE Select NP_000660.1:n.829-228G=
NR_133005.2:n.856-228G= (ADH1C)