Canonical Allele Identifier: CA1868280491
Gene: ALDOB HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101428454G= , CM000671.2:g.101428454G= GRCh38
NC_000009.11:g.104190736G= , CM000671.1:g.104190736G= GRCh37
NC_000009.10:g.103230557G= NCBI36
NG_012387.1:g.12327C=

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.379+15C= MANE Select ENSP00000497767.1:n.379+15C=
ENST00000648064.1:c.379+15C= ENSP00000497990.1:n.379+15C=
ENST00000648758.1:c.379+15C= ENSP00000497731.1:n.379+15C=
ENST00000649902.1:c.379+15C= ENSP00000497216.1:n.379+15C=
ENST00000374855.8:c.379+15C= ENSP00000363988.4:n.379+15C=
ENST00000468981.3:n.67+1355C=
ENST00000616752.1:c.379+15C= ENSP00000481363.1:n.379+15C=
NM_000035.3:c.379+15C= NP_000026.2:n.379+15C=
NM_000035.4:c.379+15C= MANE Select NP_000026.2:n.379+15C=
Search 100 bp 5'
Search 100 bp 3'