Canonical Allele Identifier: CA374264081
Gene: ALDOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.104184159A>C (hg19) chr9:g.101421877A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421877A>C , CM000671.2:g.101421877A>C GRCh38
NC_000009.11:g.104184159A>C , CM000671.1:g.104184159A>C GRCh37
NC_000009.10:g.103223980A>C NCBI36
NG_012387.1:g.18904T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.1027T>G MANE Select ENSP00000497767.1:p.Tyr343Asp
ENST00000648064.1:c.1027T>G ENSP00000497990.1:p.Tyr343Asp
ENST00000648758.1:c.1027T>G ENSP00000497731.1:p.Tyr343Asp
ENST00000374855.8:c.1027T>G ENSP00000363988.4:p.Tyr343Asp
ENST00000616752.1:c.*39T>G ENSP00000481363.1:n.*39T>G
NM_000035.3:c.1027T>G NP_000026.2:p.Tyr343Asp
NM_000035.4:c.1027T>G MANE Select NP_000026.2:p.Tyr343Asp
Search 100 bp 5'
Search 100 bp 3'