Canonical Allele Identifier: CA196955806
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1803088
gnomAD v2: 9-104184117-G-C
gnomAD v4: 9-101421835-G-C
MyVariant Identifiers: chr9:g.104184117G>C (hg19) chr9:g.101421835G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421835G>C , CM000671.2:g.101421835G>C GRCh38
NC_000009.11:g.104184117G>C , CM000671.1:g.104184117G>C GRCh37
NC_000009.10:g.103223938G>C NCBI36
NG_012387.1:g.18946C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.1069C>G MANE Select ENSP00000497767.1:p.Leu357Val
ENST00000648064.1:c.1069C>G ENSP00000497990.1:p.Leu357Val
ENST00000648758.1:c.1069C>G ENSP00000497731.1:p.Leu357Val
ENST00000374855.8:c.1069C>G ENSP00000363988.4:p.Leu357Val
ENST00000616752.1:c.*81C>G ENSP00000481363.1:n.*81C>G
NM_000035.3:c.1069C>G NP_000026.2:p.Leu357Val
NM_000035.4:c.1069C>G MANE Select NP_000026.2:p.Leu357Val
Search 100 bp 5'
Search 100 bp 3'