Canonical Allele Identifier: CA356708539

Gene: CHRNA9

Linked Data

• MyVariant Identifiers: chr4:g.40356500T>A (hg19) ; chr4:g.40354483T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310169.3:c.1403T>A MANE Select	ENSP00000312663.2:p.Phe468Tyr
ENST00000310169.2:c.1403T>A	ENSP00000312663.2:p.Phe468Tyr
NM_017581.3:c.1403T>A	NP_060051.2:p.Phe468Tyr
NM_017581.4:c.1403T>A MANE Select	NP_060051.2:p.Phe468Tyr