Canonical Allele Identifier: CA196957525
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs761814594
MyVariant Identifiers: chr9:g.104190215G>C (hg19) chr9:g.101427933G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101427933G>C , CM000671.2:g.101427933G>C GRCh38
NC_000009.11:g.104190215G>C , CM000671.1:g.104190215G>C GRCh37
NC_000009.10:g.103230036G>C NCBI36
NG_012387.1:g.12848C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.380-291C>G MANE Select ENSP00000497767.1:n.380-291C>G
ENST00000648064.1:c.380-291C>G ENSP00000497990.1:n.380-291C>G
ENST00000648758.1:c.380-291C>G ENSP00000497731.1:n.380-291C>G
ENST00000649902.1:c.380-291C>G ENSP00000497216.1:n.380-291C>G
ENST00000374855.8:c.380-291C>G ENSP00000363988.4:n.380-291C>G
ENST00000468981.3:n.68-1295C>G
ENST00000616752.1:c.380-291C>G ENSP00000481363.1:n.380-291C>G
NM_000035.3:c.380-291C>G NP_000026.2:n.380-291C>G
NM_000035.4:c.380-291C>G MANE Select NP_000026.2:n.380-291C>G
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