Canonical Allele Identifier: CA374264890
Gene: ALDOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425593T>G , CM000671.2:g.101425593T>G GRCh38
NC_000009.11:g.104187875T>G , CM000671.1:g.104187875T>G GRCh37
NC_000009.10:g.103227696T>G NCBI36
NG_012387.1:g.15188A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.659A>C MANE Select ENSP00000497767.1:p.His220Pro
ENST00000648064.1:c.659A>C ENSP00000497990.1:p.His220Pro
ENST00000648758.1:c.659A>C ENSP00000497731.1:p.His220Pro
ENST00000649902.1:c.659A>C ENSP00000497216.1:p.His220Pro
ENST00000374855.8:c.659A>C ENSP00000363988.4:p.His220Pro
ENST00000468981.3:n.186A>C
ENST00000616752.1:c.659A>C ENSP00000481363.1:p.His220Pro
NM_000035.3:c.659A>C NP_000026.2:p.His220Pro
NM_000035.4:c.659A>C MANE Select NP_000026.2:p.His220Pro