Canonical Allele Identifier: CA2691006238
Gene: ALDOB HGNC NCBI

Linked Data

gnomAD v4: 9-101421527-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421527T>G , CM000671.2:g.101421527T>G GRCh38
NC_000009.11:g.104183809T>G , CM000671.1:g.104183809T>G GRCh37
NC_000009.10:g.103223630T>G NCBI36
NG_012387.1:g.19254A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*282A>C MANE Select ENSP00000497767.1:n.*282A>C
ENST00000648064.1:c.*282A>C ENSP00000497990.1:n.*282A>C
ENST00000374855.8:c.*282A>C ENSP00000363988.4:n.*282A>C
NM_000035.3:c.*282A>C NP_000026.2:n.*282A>C
NM_000035.4:c.*282A>C MANE Select NP_000026.2:n.*282A>C
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