Canonical Allele Identifier: CA2739994256
Gene: ALDOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421798G>A , CM000671.2:g.101421798G>A GRCh38
NC_000009.11:g.104184080G>A , CM000671.1:g.104184080G>A GRCh37
NC_000009.10:g.103223901G>A NCBI36
NG_012387.1:g.18983C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.*11C>T MANE Select ENSP00000497767.1:n.*11C>T
ENST00000648064.1:c.*11C>T ENSP00000497990.1:n.*11C>T
ENST00000648758.1:c.*11C>T ENSP00000497731.1:n.*11C>T
ENST00000374855.8:c.*11C>T ENSP00000363988.4:n.*11C>T
ENST00000616752.1:c.*118C>T ENSP00000481363.1:n.*118C>T
NM_000035.3:c.*11C>T NP_000026.2:n.*11C>T
NM_000035.4:c.*11C>T MANE Select NP_000026.2:n.*11C>T
Search 100 bp 5'
Search 100 bp 3'