Canonical Allele Identifier: CA374266303
Gene: ALDOB HGNC NCBI
MyVariant.info:
Revel Score:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101430878G>C , CM000671.2:g.101430878G>C GRCh38
NC_000009.11:g.104193160G>C , CM000671.1:g.104193160G>C GRCh37
NC_000009.10:g.103232981G>C NCBI36
NG_012387.1:g.9903C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.10C>G MANE Select ENSP00000497767.1:p.Arg4Gly
ENST00000648064.1:c.10C>G ENSP00000497990.1:p.Arg4Gly
ENST00000648423.1:c.10C>G ENSP00000497985.1:p.Arg4Gly
ENST00000648758.1:c.10C>G ENSP00000497731.1:p.Arg4Gly
ENST00000648906.1:n.180C>G
ENST00000649902.1:c.10C>G ENSP00000497216.1:p.Arg4Gly
ENST00000650613.1:n.86C>G
ENST00000374855.8:c.10C>G ENSP00000363988.4:p.Arg4Gly
ENST00000616752.1:c.10C>G ENSP00000481363.1:p.Arg4Gly
NM_000035.3:c.10C>G NP_000026.2:p.Arg4Gly
NM_000035.4:c.10C>G MANE Select NP_000026.2:p.Arg4Gly