Canonical Allele Identifier: CA2691006174
Gene: ALDOB HGNC NCBI

Linked Data

gnomAD v4: 9-101421408-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421408G>T , CM000671.2:g.101421408G>T GRCh38
NC_000009.11:g.104183690G>T , CM000671.1:g.104183690G>T GRCh37
NC_000009.10:g.103223511G>T NCBI36
NG_012387.1:g.19373C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*401C>A MANE Select ENSP00000497767.1:n.*401C>A
ENST00000374855.8:c.*401C>A ENSP00000363988.4:n.*401C>A
NM_000035.3:c.*401C>A NP_000026.2:n.*401C>A
NM_000035.4:c.*401C>A MANE Select NP_000026.2:n.*401C>A
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