Canonical Allele Identifier: CA357498683
Gene: ADH7 HGNC NCBI

Linked Data

dbSNP Id: rs1254796684
gnomAD v4: 4-99428551-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99428551C>T , CM000666.2:g.99428551C>T GRCh38
NC_000004.11:g.100349708C>T , CM000666.1:g.100349708C>T GRCh37
NC_000004.10:g.100568731C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.200G>A MANE Select ENSP00000414254.2:p.Gly67Glu
ENST00000209665.8:c.236G>A ENSP00000209665.4:p.Gly79Glu
ENST00000437033.6:c.200G>A ENSP00000414254.2:p.Gly67Glu
ENST00000474027.1:c.29G>A ENSP00000420300.1:p.Gly10Glu
ENST00000476959.5:c.260G>A ENSP00000420269.1:p.Gly87Glu
ENST00000482593.5:c.29G>A ENSP00000420613.1:p.Gly10Glu
NM_000673.4:c.236G>A NP_000664.2:p.Gly79Glu
NM_001166504.1:c.260G>A NP_001159976.1:p.Gly87Glu
NM_000673.7:c.200G>A MANE Select NP_000664.3:p.Gly67Glu
NM_001166504.2:c.260G>A NP_001159976.1:p.Gly87Glu