Canonical Allele Identifier: CA356706530

Gene: CHRNA9

Linked Data

• dbSNP Id: rs1481883054
• gnomAD v2: 4-40356327-C-A
• gnomAD v4: 4-40354310-C-A
• MyVariant Identifiers: chr4:g.40356327C>A (hg19) ; chr4:g.40354310C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.40354310C>A , CM000666.2:g.40354310C>A	GRCh38
NC_000004.11:g.40356327C>A , CM000666.1:g.40356327C>A	GRCh37
NC_000004.10:g.40051084C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000310169.3:c.1230C>A MANE Select	ENSP00000312663.2:p.Asn410Lys
ENST00000310169.2:c.1230C>A	ENSP00000312663.2:p.Asn410Lys
NM_017581.3:c.1230C>A	NP_060051.2:p.Asn410Lys
NM_017581.4:c.1230C>A MANE Select	NP_060051.2:p.Asn410Lys