Canonical Allele Identifier: CA196955672
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs996768943
gnomAD v3: 9-101421538-C-T
gnomAD v4: 9-101421538-C-T
MyVariant Identifiers: chr9:g.104183820C>T (hg19) chr9:g.101421538C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421538C>T , CM000671.2:g.101421538C>T GRCh38
NC_000009.11:g.104183820C>T , CM000671.1:g.104183820C>T GRCh37
NC_000009.10:g.103223641C>T NCBI36
NG_012387.1:g.19243G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*271G>A MANE Select ENSP00000497767.1:n.*271G>A
ENST00000648064.1:c.*271G>A ENSP00000497990.1:n.*271G>A
ENST00000374855.8:c.*271G>A ENSP00000363988.4:n.*271G>A
NM_000035.3:c.*271G>A NP_000026.2:n.*271G>A
NM_000035.4:c.*271G>A MANE Select NP_000026.2:n.*271G>A
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