Canonical Allele Identifier: CA196955629
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1042042177
gnomAD v2: 9-104183729-T-A
gnomAD v3: 9-101421447-T-A
gnomAD v4: 9-101421447-T-A
MyVariant Identifiers: chr9:g.104183729T>A (hg19) chr9:g.101421447T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421447T>A , CM000671.2:g.101421447T>A GRCh38
NC_000009.11:g.104183729T>A , CM000671.1:g.104183729T>A GRCh37
NC_000009.10:g.103223550T>A NCBI36
NG_012387.1:g.19334A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*362A>T MANE Select ENSP00000497767.1:n.*362A>T
ENST00000648064.1:c.*362A>T ENSP00000497990.1:n.*362A>T
ENST00000374855.8:c.*362A>T ENSP00000363988.4:n.*362A>T
NM_000035.3:c.*362A>T NP_000026.2:n.*362A>T
NM_000035.4:c.*362A>T MANE Select NP_000026.2:n.*362A>T
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