Canonical Allele Identifier: CA374264138
Gene: ALDOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421903G>C , CM000671.2:g.101421903G>C GRCh38
NC_000009.11:g.104184185G>C , CM000671.1:g.104184185G>C GRCh37
NC_000009.10:g.103224006G>C NCBI36
NG_012387.1:g.18878C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.1001C>G MANE Select ENSP00000497767.1:p.Ala334Gly
ENST00000648064.1:c.1001C>G ENSP00000497990.1:p.Ala334Gly
ENST00000648758.1:c.1001C>G ENSP00000497731.1:p.Ala334Gly
ENST00000374855.8:c.1001C>G ENSP00000363988.4:p.Ala334Gly
ENST00000616752.1:c.*13C>G ENSP00000481363.1:n.*13C>G
NM_000035.3:c.1001C>G NP_000026.2:p.Ala334Gly
NM_000035.4:c.1001C>G MANE Select NP_000026.2:p.Ala334Gly