Canonical Allele Identifier: CA357497350
Gene: ADH7 HGNC NCBI

Linked Data

dbSNP Id: rs1251197589
MyVariant Identifiers: chr4:g.100341692T>G (hg19) chr4:g.99420535T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420535T>G , CM000666.2:g.99420535T>G GRCh38
NC_000004.11:g.100341692T>G , CM000666.1:g.100341692T>G GRCh37
NC_000004.10:g.100560715T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.823A>C MANE Select ENSP00000414254.2:p.Met275Leu
ENST00000209665.8:c.859A>C ENSP00000209665.4:p.Met287Leu
ENST00000437033.6:c.823A>C ENSP00000414254.2:p.Met275Leu
ENST00000476959.5:c.883A>C ENSP00000420269.1:p.Met295Leu
ENST00000482593.5:c.652A>C ENSP00000420613.1:p.Met218Leu
NM_000673.4:c.859A>C NP_000664.2:p.Met287Leu
NM_001166504.1:c.883A>C NP_001159976.1:p.Met295Leu
NM_000673.7:c.823A>C MANE Select NP_000664.3:p.Met275Leu
NM_001166504.2:c.883A>C NP_001159976.1:p.Met295Leu
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