Canonical Allele Identifier: CA1868275539
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1831050596
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421788T>G , CM000671.2:g.101421788T>G GRCh38
NC_000009.11:g.104184070T>G , CM000671.1:g.104184070T>G GRCh37
NC_000009.10:g.103223891T>G NCBI36
NG_012387.1:g.18993A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.*21A>C MANE Select ENSP00000497767.1:n.*21A>C
ENST00000648064.1:c.*21A>C ENSP00000497990.1:n.*21A>C
ENST00000648758.1:c.*21A>C ENSP00000497731.1:n.*21A>C
ENST00000374855.8:c.*21A>C ENSP00000363988.4:n.*21A>C
ENST00000616752.1:c.*128A>C ENSP00000481363.1:n.*128A>C
NM_000035.3:c.*21A>C NP_000026.2:n.*21A>C
NM_000035.4:c.*21A>C MANE Select NP_000026.2:n.*21A>C
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