Canonical Allele Identifier: CA356705656

Gene: CHRNA9

Linked Data

• MyVariant Identifiers: chr4:g.40356169T>C (hg19) ; chr4:g.40354152T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.40354152T>C , CM000666.2:g.40354152T>C	GRCh38
NC_000004.11:g.40356169T>C , CM000666.1:g.40356169T>C	GRCh37
NC_000004.10:g.40050926T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310169.3:c.1072T>C MANE Select	ENSP00000312663.2:p.Cys358Arg
ENST00000310169.2:c.1072T>C	ENSP00000312663.2:p.Cys358Arg
NM_017581.3:c.1072T>C	NP_060051.2:p.Cys358Arg
NM_017581.4:c.1072T>C MANE Select	NP_060051.2:p.Cys358Arg