Canonical Allele Identifier: CA356706533
Gene: CHRNA9 HGNC NCBI

Linked Data

dbSNP Id: rs1712890659
gnomAD v4: 4-40354311-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354311C>G , CM000666.2:g.40354311C>G GRCh38
NC_000004.11:g.40356328C>G , CM000666.1:g.40356328C>G GRCh37
NC_000004.10:g.40051085C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000310169.3:c.1231C>G MANE Select ENSP00000312663.2:p.Pro411Ala
ENST00000310169.2:c.1231C>G ENSP00000312663.2:p.Pro411Ala
NM_017581.3:c.1231C>G NP_060051.2:p.Pro411Ala
NM_017581.4:c.1231C>G MANE Select NP_060051.2:p.Pro411Ala