Canonical Allele Identifier: CA1452583931
Gene: CHRNA9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354319G= , CM000666.2:g.40354319G= GRCh38
NC_000004.11:g.40356336G= , CM000666.1:g.40356336G= GRCh37
NC_000004.10:g.40051093G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.1239G= MANE Select ENSP00000312663.2:p.Glu413=
ENST00000310169.2:c.1239G= ENSP00000312663.2:p.Glu413=
NM_017581.3:c.1239G= NP_060051.2:p.Glu413=
NM_017581.4:c.1239G= MANE Select NP_060051.2:p.Glu413=