Canonical Allele Identifier: CA466462964
Gene: ALDOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.104190779T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101428497T>G , CM000671.2:g.101428497T>G GRCh38
NC_000009.11:g.104190779T>G , CM000671.1:g.104190779T>G GRCh37
NC_000009.10:g.103230600T>G NCBI36
NG_012387.1:g.12284A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.351A>C MANE Select ENSP00000497767.1:p.Ala117=
ENST00000648064.1:c.351A>C ENSP00000497990.1:p.Ala117=
ENST00000648758.1:c.351A>C ENSP00000497731.1:p.Ala117=
ENST00000649902.1:c.351A>C ENSP00000497216.1:p.Ala117=
ENST00000374855.8:c.351A>C ENSP00000363988.4:p.Ala117=
ENST00000468981.3:n.67+1312A>C
ENST00000616752.1:c.351A>C ENSP00000481363.1:p.Ala117=
NM_000035.3:c.351A>C NP_000026.2:p.Ala117=
NM_000035.4:c.351A>C MANE Select NP_000026.2:p.Ala117=
Search 100 bp 5'
Search 100 bp 3'