Canonical Allele Identifier: CA1868275418
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421689T= , CM000671.2:g.101421689T= GRCh38
NC_000009.11:g.104183971T= , CM000671.1:g.104183971T= GRCh37
NC_000009.10:g.103223792T= NCBI36
NG_012387.1:g.19092A=

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.*120A= MANE Select ENSP00000497767.1:n.*120A=
ENST00000648064.1:c.*120A= ENSP00000497990.1:n.*120A=
ENST00000648758.1:c.*120A= ENSP00000497731.1:n.*120A=
ENST00000374855.8:c.*120A= ENSP00000363988.4:n.*120A=
ENST00000616752.1:c.*227A= ENSP00000481363.1:n.*227A=
NM_000035.3:c.*120A= NP_000026.2:n.*120A=
NM_000035.4:c.*120A= MANE Select NP_000026.2:n.*120A=