Canonical Allele Identifier: CA1868275336
Gene: ALDOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421615A= , CM000671.2:g.101421615A= GRCh38
NC_000009.11:g.104183897A= , CM000671.1:g.104183897A= GRCh37
NC_000009.10:g.103223718A= NCBI36
NG_012387.1:g.19166T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*194T= MANE Select ENSP00000497767.1:n.*194T=
ENST00000648064.1:c.*194T= ENSP00000497990.1:n.*194T=
ENST00000374855.8:c.*194T= ENSP00000363988.4:n.*194T=
ENST00000616752.1:c.*301T= ENSP00000481363.1:n.*301T=
NM_000035.3:c.*194T= NP_000026.2:n.*194T=
NM_000035.4:c.*194T= MANE Select NP_000026.2:n.*194T=
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