Canonical Allele Identifier: CA95758527

Gene: CHRNA9

Linked Data

• dbSNP Id: rs1044783303
• gnomAD v2: 4-40356539-C-G
• gnomAD v4: 4-40354522-C-G
• MyVariant Identifiers: chr4:g.40356539C>G (hg19) ; chr4:g.40354522C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.40354522C>G , CM000666.2:g.40354522C>G	GRCh38
NC_000004.11:g.40356539C>G , CM000666.1:g.40356539C>G	GRCh37
NC_000004.10:g.40051296C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310169.3:c.*2C>G MANE Select	ENSP00000312663.2:n.*2C>G
ENST00000310169.2:c.*2C>G	ENSP00000312663.2:n.*2C>G
NM_017581.3:c.*2C>G	NP_060051.2:n.*2C>G
NM_017581.4:c.*2C>G MANE Select	NP_060051.2:n.*2C>G