Canonical Allele Identifier: CA439141445
Gene: CHRNA9 HGNC NCBI

Linked Data

dbSNP Id: rs777050492
gnomAD v2: 4-40356336-G-A
gnomAD v4: 4-40354319-G-A

Genomic Alleles

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

Transcript Alleles

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