Canonical Allele Identifier: CA95746644
Gene: CHRNA9 HGNC NCBI

Linked Data

dbSNP Id: rs6819385
gnomAD v2: 4-40339574-A-G
gnomAD v3: 4-40337557-A-G
gnomAD v4: 4-40337557-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40337557A>G , CM000666.2:g.40337557A>G GRCh38
NC_000004.11:g.40339574A>G , CM000666.1:g.40339574A>G GRCh37
NC_000004.10:g.40034331A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000310169.3:c.365+193A>G MANE Select ENSP00000312663.2:n.365+193A>G
ENST00000310169.2:c.365+193A>G ENSP00000312663.2:n.365+193A>G
ENST00000502377.1:n.79+193A>G
NM_017581.3:c.365+193A>G NP_060051.2:n.365+193A>G
NM_017581.4:c.365+193A>G MANE Select NP_060051.2:n.365+193A>G