Canonical Allele Identifier: CA356708539
Gene: CHRNA9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354483T>A , CM000666.2:g.40354483T>A GRCh38
NC_000004.11:g.40356500T>A , CM000666.1:g.40356500T>A GRCh37
NC_000004.10:g.40051257T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.1403T>A MANE Select ENSP00000312663.2:p.Phe468Tyr
ENST00000310169.2:c.1403T>A ENSP00000312663.2:p.Phe468Tyr
NM_017581.3:c.1403T>A NP_060051.2:p.Phe468Tyr
NM_017581.4:c.1403T>A MANE Select NP_060051.2:p.Phe468Tyr