Canonical Allele Identifier: CA1868281084
Gene: ALDOB HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101429752C= , CM000671.2:g.101429752C= GRCh38
NC_000009.11:g.104192034C= , CM000671.1:g.104192034C= GRCh37
NC_000009.10:g.103231855C= NCBI36
NG_012387.1:g.11029G=

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.324+3G= MANE Select ENSP00000497767.1:n.324+3G=
ENST00000648064.1:c.324+3G= ENSP00000497990.1:n.324+3G=
ENST00000648758.1:c.324+3G= ENSP00000497731.1:n.324+3G=
ENST00000648906.1:n.497G=
ENST00000649902.1:c.324+3G= ENSP00000497216.1:n.324+3G=
ENST00000650613.1:n.403G=
ENST00000374855.8:c.324+3G= ENSP00000363988.4:n.324+3G=
ENST00000468981.3:n.67+57G=
ENST00000616752.1:c.324+3G= ENSP00000481363.1:n.324+3G=
NM_000035.3:c.324+3G= NP_000026.2:n.324+3G=
NM_000035.4:c.324+3G= MANE Select NP_000026.2:n.324+3G=
Search 100 bp 5'
Search 100 bp 3'