Canonical Allele Identifier: CA589815519
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1188485332
gnomAD v2: 9-104184076-G-A
gnomAD v4: 9-101421794-G-A
MyVariant Identifiers: chr9:g.104184076G>A (hg19) chr9:g.101421794G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421794G>A , CM000671.2:g.101421794G>A GRCh38
NC_000009.11:g.104184076G>A , CM000671.1:g.104184076G>A GRCh37
NC_000009.10:g.103223897G>A NCBI36
NG_012387.1:g.18987C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.*15C>T MANE Select ENSP00000497767.1:n.*15C>T
ENST00000648064.1:c.*15C>T ENSP00000497990.1:n.*15C>T
ENST00000648758.1:c.*15C>T ENSP00000497731.1:n.*15C>T
ENST00000374855.8:c.*15C>T ENSP00000363988.4:n.*15C>T
ENST00000616752.1:c.*122C>T ENSP00000481363.1:n.*122C>T
NM_000035.3:c.*15C>T NP_000026.2:n.*15C>T
NM_000035.4:c.*15C>T MANE Select NP_000026.2:n.*15C>T
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