Canonical Allele Identifier: CA356705899

Gene: CHRNA9

Linked Data

• MyVariant Identifiers: chr4:g.40356222C>G (hg19) ; chr4:g.40354205C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.40354205C>G , CM000666.2:g.40354205C>G	GRCh38
NC_000004.11:g.40356222C>G , CM000666.1:g.40356222C>G	GRCh37
NC_000004.10:g.40050979C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310169.3:c.1125C>G MANE Select	ENSP00000312663.2:p.Ser375Arg
ENST00000310169.2:c.1125C>G	ENSP00000312663.2:p.Ser375Arg
NM_017581.3:c.1125C>G	NP_060051.2:p.Ser375Arg
NM_017581.4:c.1125C>G MANE Select	NP_060051.2:p.Ser375Arg