Canonical Allele Identifier: CA374264443
Gene: ALDOB HGNC NCBI

Linked Data

gnomAD v4: 9-101424968-G-T
MyVariant Identifiers: chr9:g.104187250G>T (hg19) chr9:g.101424968G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101424968G>T , CM000671.2:g.101424968G>T GRCh38
NC_000009.11:g.104187250G>T , CM000671.1:g.104187250G>T GRCh37
NC_000009.10:g.103227071G>T NCBI36
NG_012387.1:g.15813C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.874C>A MANE Select ENSP00000497767.1:p.Leu292Ile
ENST00000648064.1:c.874C>A ENSP00000497990.1:p.Leu292Ile
ENST00000648758.1:c.874C>A ENSP00000497731.1:p.Leu292Ile
ENST00000649902.1:c.874C>A ENSP00000497216.1:p.Leu292Ile
ENST00000374855.8:c.874C>A ENSP00000363988.4:p.Leu292Ile
ENST00000616752.1:c.874C>A ENSP00000481363.1:p.Leu292Ile
NM_000035.3:c.874C>A NP_000026.2:p.Leu292Ile
NM_000035.4:c.874C>A MANE Select NP_000026.2:p.Leu292Ile
Search 100 bp 5'
Search 100 bp 3'