Canonical Allele Identifier: CA374264817
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1831115893

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425557T>C , CM000671.2:g.101425557T>C GRCh38
NC_000009.11:g.104187839T>C , CM000671.1:g.104187839T>C GRCh37
NC_000009.10:g.103227660T>C NCBI36
NG_012387.1:g.15224A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.695A>G MANE Select ENSP00000497767.1:p.Asn232Ser
ENST00000648064.1:c.695A>G ENSP00000497990.1:p.Asn232Ser
ENST00000648758.1:c.695A>G ENSP00000497731.1:p.Asn232Ser
ENST00000649902.1:c.695A>G ENSP00000497216.1:p.Asn232Ser
ENST00000374855.8:c.695A>G ENSP00000363988.4:p.Asn232Ser
ENST00000616752.1:c.695A>G ENSP00000481363.1:p.Asn232Ser
NM_000035.3:c.695A>G NP_000026.2:p.Asn232Ser
NM_000035.4:c.695A>G MANE Select NP_000026.2:p.Asn232Ser