Canonical Allele Identifier: CA374264276
Gene: ALDOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.104187173C>G (hg19) chr9:g.101424891C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101424891C>G , CM000671.2:g.101424891C>G GRCh38
NC_000009.11:g.104187173C>G , CM000671.1:g.104187173C>G GRCh37
NC_000009.10:g.103226994C>G NCBI36
NG_012387.1:g.15890G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.951G>C MANE Select ENSP00000497767.1:p.Lys317Asn
ENST00000648064.1:c.951G>C ENSP00000497990.1:p.Lys317Asn
ENST00000648758.1:c.951G>C ENSP00000497731.1:p.Lys317Asn
ENST00000649902.1:c.951G>C ENSP00000497216.1:p.Lys317Asn
ENST00000374855.8:c.951G>C ENSP00000363988.4:p.Lys317Asn
ENST00000616752.1:c.914G>C ENSP00000481363.1:p.Arg305Thr
NM_000035.3:c.951G>C NP_000026.2:p.Lys317Asn
NM_000035.4:c.951G>C MANE Select NP_000026.2:p.Lys317Asn
Search 100 bp 5'
Search 100 bp 3'