Canonical Allele Identifier: CA357498720
Gene: ADH7 HGNC NCBI

Linked Data

dbSNP Id: rs1464469225
gnomAD v4: 4-99428569-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99428569T>C , CM000666.2:g.99428569T>C GRCh38
NC_000004.11:g.100349726T>C , CM000666.1:g.100349726T>C GRCh37
NC_000004.10:g.100568749T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.182A>G MANE Select ENSP00000414254.2:p.Lys61Arg
ENST00000209665.8:c.218A>G ENSP00000209665.4:p.Lys73Arg
ENST00000437033.6:c.182A>G ENSP00000414254.2:p.Lys61Arg
ENST00000474027.1:c.11A>G ENSP00000420300.1:p.Lys4Arg
ENST00000476959.5:c.242A>G ENSP00000420269.1:p.Lys81Arg
ENST00000482593.5:c.11A>G ENSP00000420613.1:p.Lys4Arg
NM_000673.4:c.218A>G NP_000664.2:p.Lys73Arg
NM_001166504.1:c.242A>G NP_001159976.1:p.Lys81Arg
NM_000673.7:c.182A>G MANE Select NP_000664.3:p.Lys61Arg
NM_001166504.2:c.242A>G NP_001159976.1:p.Lys81Arg