Canonical Allele Identifier: CA95758353
Gene: CHRNA9 HGNC NCBI

Linked Data

dbSNP Id: rs267600154
gnomAD v4: 4-40354306-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354306A>G , CM000666.2:g.40354306A>G GRCh38
NC_000004.11:g.40356323A>G , CM000666.1:g.40356323A>G GRCh37
NC_000004.10:g.40051080A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000310169.3:c.1226A>G MANE Select ENSP00000312663.2:p.Lys409Arg
ENST00000310169.2:c.1226A>G ENSP00000312663.2:p.Lys409Arg
NM_017581.3:c.1226A>G NP_060051.2:p.Lys409Arg
NM_017581.4:c.1226A>G MANE Select NP_060051.2:p.Lys409Arg