Canonical Allele Identifier: CA1868275818
Gene: ALDOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421947T= , CM000671.2:g.101421947T= GRCh38
NC_000009.11:g.104184229T= , CM000671.1:g.104184229T= GRCh37
NC_000009.10:g.103224050T= NCBI36
NG_012387.1:g.18834A=

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.1000-43A= MANE Select ENSP00000497767.1:n.1000-43A=
ENST00000648064.1:c.1000-43A= ENSP00000497990.1:n.1000-43A=
ENST00000648758.1:c.1000-43A= ENSP00000497731.1:n.1000-43A=
ENST00000374855.8:c.1000-43A= ENSP00000363988.4:n.1000-43A=
ENST00000616752.1:c.*12-43A= ENSP00000481363.1:n.*12-43A=
NM_000035.3:c.1000-43A= NP_000026.2:n.1000-43A=
NM_000035.4:c.1000-43A= MANE Select NP_000026.2:n.1000-43A=
Search 100 bp 5'
Search 100 bp 3'