Canonical Allele Identifier: CA1868280974
Gene: ALDOB HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101429486T= , CM000671.2:g.101429486T= GRCh38
NC_000009.11:g.104191768T= , CM000671.1:g.104191768T= GRCh37
NC_000009.10:g.103231589T= NCBI36
NG_012387.1:g.11295A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.324+269A= MANE Select ENSP00000497767.1:n.324+269A=
ENST00000648064.1:c.324+269A= ENSP00000497990.1:n.324+269A=
ENST00000648758.1:c.324+269A= ENSP00000497731.1:n.324+269A=
ENST00000648906.1:n.763A=
ENST00000649902.1:c.324+269A= ENSP00000497216.1:n.324+269A=
ENST00000650613.1:n.669A=
ENST00000374855.8:c.324+269A= ENSP00000363988.4:n.324+269A=
ENST00000468981.3:n.67+323A=
ENST00000616752.1:c.324+269A= ENSP00000481363.1:n.324+269A=
NM_000035.3:c.324+269A= NP_000026.2:n.324+269A=
NM_000035.4:c.324+269A= MANE Select NP_000026.2:n.324+269A=
Search 100 bp 5'
Search 100 bp 3'