Canonical Allele Identifier: CA2691005959
Gene: ALDOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101429670T>A , CM000671.2:g.101429670T>A GRCh38
NC_000009.11:g.104191952T>A , CM000671.1:g.104191952T>A GRCh37
NC_000009.10:g.103231773T>A NCBI36
NG_012387.1:g.11111A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.324+85A>T MANE Select ENSP00000497767.1:n.324+85A>T
ENST00000648064.1:c.324+85A>T ENSP00000497990.1:n.324+85A>T
ENST00000648758.1:c.324+85A>T ENSP00000497731.1:n.324+85A>T
ENST00000648906.1:n.579A>T
ENST00000649902.1:c.324+85A>T ENSP00000497216.1:n.324+85A>T
ENST00000650613.1:n.485A>T
ENST00000374855.8:c.324+85A>T ENSP00000363988.4:n.324+85A>T
ENST00000468981.3:n.67+139A>T
ENST00000616752.1:c.324+85A>T ENSP00000481363.1:n.324+85A>T
NM_000035.3:c.324+85A>T NP_000026.2:n.324+85A>T
NM_000035.4:c.324+85A>T MANE Select NP_000026.2:n.324+85A>T