Canonical Allele Identifier: CA196955753
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs977848157
gnomAD v2: 9-104184015-C-T
gnomAD v3: 9-101421733-C-T
gnomAD v4: 9-101421733-C-T
MyVariant Identifiers: chr9:g.104184015C>T (hg19) chr9:g.101421733C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421733C>T , CM000671.2:g.101421733C>T GRCh38
NC_000009.11:g.104184015C>T , CM000671.1:g.104184015C>T GRCh37
NC_000009.10:g.103223836C>T NCBI36
NG_012387.1:g.19048G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.*76G>A MANE Select ENSP00000497767.1:n.*76G>A
ENST00000648064.1:c.*76G>A ENSP00000497990.1:n.*76G>A
ENST00000648758.1:c.*76G>A ENSP00000497731.1:n.*76G>A
ENST00000374855.8:c.*76G>A ENSP00000363988.4:n.*76G>A
ENST00000616752.1:c.*183G>A ENSP00000481363.1:n.*183G>A
NM_000035.3:c.*76G>A NP_000026.2:n.*76G>A
NM_000035.4:c.*76G>A MANE Select NP_000026.2:n.*76G>A
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