Canonical Allele Identifier: CA5500030
Gene: NCOA4 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10761581

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46027444A>C , CM000672.2:g.46027444A>C GRCh38
NC_000010.9:g.51238384T>G NCBI36
NC_000010.10:g.51568378T>G , CM000672.1:g.51568378T>G GRCh37
NG_023372.1:g.8271T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000578454.5:c.22T>G ENSP00000463027.1:p.Phe8Val
ENST00000579039.2:c.22T>G ENSP00000463455.1:p.Phe8Val
ENST00000580070.5:c.-128+3082T>G ENSP00000462352.1:p.=
ENST00000581486.5:c.-15+3082T>G ENSP00000462943.1:p.=
ENST00000585056.5:c.-71+3082T>G ENSP00000463022.1:p.=
NM_001145260.1:c.22T>G NP_001138732.1:p.Phe8Val
NM_001145261.1:c.22T>G NP_001138733.1:p.Phe8Val
NM_001145263.1:c.-15+3082T>G NP_001138735.1:p.=