Canonical Allele Identifier: CA374265372
Gene: ALDOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.104189872G>C (hg19) chr9:g.101427590G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101427590G>C , CM000671.2:g.101427590G>C GRCh38
NC_000009.11:g.104189872G>C , CM000671.1:g.104189872G>C GRCh37
NC_000009.10:g.103229693G>C NCBI36
NG_012387.1:g.13191C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.432C>G MANE Select ENSP00000497767.1:p.Asp144Glu
ENST00000648064.1:c.432C>G ENSP00000497990.1:p.Asp144Glu
ENST00000648758.1:c.432C>G ENSP00000497731.1:p.Asp144Glu
ENST00000649902.1:c.432C>G ENSP00000497216.1:p.Asp144Glu
ENST00000374855.8:c.432C>G ENSP00000363988.4:p.Asp144Glu
ENST00000468981.3:n.68-952C>G
ENST00000616752.1:c.432C>G ENSP00000481363.1:p.Asp144Glu
NM_000035.3:c.432C>G NP_000026.2:p.Asp144Glu
NM_000035.4:c.432C>G MANE Select NP_000026.2:p.Asp144Glu
Search 100 bp 5'
Search 100 bp 3'