Canonical Allele Identifier: CA356708547

Gene: CHRNA9

Linked Data

• dbSNP Id: rs1360785485
• gnomAD v3: 4-40354483-T-G
• gnomAD v4: 4-40354483-T-G
• MyVariant Identifiers: chr4:g.40356500T>G (hg19) ; chr4:g.40354483T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.40354483T>G , CM000666.2:g.40354483T>G	GRCh38
NC_000004.11:g.40356500T>G , CM000666.1:g.40356500T>G	GRCh37
NC_000004.10:g.40051257T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310169.3:c.1403T>G MANE Select	ENSP00000312663.2:p.Phe468Cys
ENST00000310169.2:c.1403T>G	ENSP00000312663.2:p.Phe468Cys
NM_017581.3:c.1403T>G	NP_060051.2:p.Phe468Cys
NM_017581.4:c.1403T>G MANE Select	NP_060051.2:p.Phe468Cys