Canonical Allele Identifier: CA1127395774
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1488672796
gnomAD v3: 9-101421778-G-A
gnomAD v4: 9-101421778-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421778G>A , CM000671.2:g.101421778G>A GRCh38
NC_000009.11:g.104184060G>A , CM000671.1:g.104184060G>A GRCh37
NC_000009.10:g.103223881G>A NCBI36
NG_012387.1:g.19003C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.*31C>T MANE Select ENSP00000497767.1:n.*31C>T
ENST00000648064.1:c.*31C>T ENSP00000497990.1:n.*31C>T
ENST00000648758.1:c.*31C>T ENSP00000497731.1:n.*31C>T
ENST00000374855.8:c.*31C>T ENSP00000363988.4:n.*31C>T
ENST00000616752.1:c.*138C>T ENSP00000481363.1:n.*138C>T
NM_000035.3:c.*31C>T NP_000026.2:n.*31C>T
NM_000035.4:c.*31C>T MANE Select NP_000026.2:n.*31C>T
Search 100 bp 5'
Search 100 bp 3'