Canonical Allele Identifier: CA356708474

Gene: CHRNA9

Linked Data

• MyVariant Identifiers: chr4:g.40356488T>A (hg19) ; chr4:g.40354471T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.40354471T>A , CM000666.2:g.40354471T>A	GRCh38
NC_000004.11:g.40356488T>A , CM000666.1:g.40356488T>A	GRCh37
NC_000004.10:g.40051245T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310169.3:c.1391T>A MANE Select	ENSP00000312663.2:p.Phe464Tyr
ENST00000310169.2:c.1391T>A	ENSP00000312663.2:p.Phe464Tyr
NM_017581.3:c.1391T>A	NP_060051.2:p.Phe464Tyr
NM_017581.4:c.1391T>A MANE Select	NP_060051.2:p.Phe464Tyr