Canonical Allele Identifier: CA374264967
Gene: ALDOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425629T>A , CM000671.2:g.101425629T>A GRCh38
NC_000009.11:g.104187911T>A , CM000671.1:g.104187911T>A GRCh37
NC_000009.10:g.103227732T>A NCBI36
NG_012387.1:g.15152A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.625-2A>T MANE Select ENSP00000497767.1:n.625-2A>T
ENST00000648064.1:c.625-2A>T ENSP00000497990.1:n.625-2A>T
ENST00000648758.1:c.625-2A>T ENSP00000497731.1:n.625-2A>T
ENST00000649902.1:c.625-2A>T ENSP00000497216.1:n.625-2A>T
ENST00000374855.8:c.625-2A>T ENSP00000363988.4:n.625-2A>T
ENST00000468981.3:n.152-2A>T
ENST00000616752.1:c.625-2A>T ENSP00000481363.1:n.625-2A>T
NM_000035.3:c.625-2A>T NP_000026.2:n.625-2A>T
NM_000035.4:c.625-2A>T MANE Select NP_000026.2:n.625-2A>T