Canonical Allele Identifier: CA374264111
Gene: ALDOB HGNC NCBI

Linked Data

COSMIC: COSM6287141
MyVariant Identifiers: chr9:g.104184174C>A (hg19) chr9:g.101421892C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421892C>A , CM000671.2:g.101421892C>A GRCh38
NC_000009.11:g.104184174C>A , CM000671.1:g.104184174C>A GRCh37
NC_000009.10:g.103223995C>A NCBI36
NG_012387.1:g.18889G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.1012G>T MANE Select ENSP00000497767.1:p.Ala338Ser
ENST00000648064.1:c.1012G>T ENSP00000497990.1:p.Ala338Ser
ENST00000648758.1:c.1012G>T ENSP00000497731.1:p.Ala338Ser
ENST00000374855.8:c.1012G>T ENSP00000363988.4:p.Ala338Ser
ENST00000616752.1:c.*24G>T ENSP00000481363.1:n.*24G>T
NM_000035.3:c.1012G>T NP_000026.2:p.Ala338Ser
NM_000035.4:c.1012G>T MANE Select NP_000026.2:p.Ala338Ser
Search 100 bp 5'
Search 100 bp 3'