Canonical Allele Identifier: CA356705742

Gene: CHRNA9

Linked Data

• gnomAD v4: 4-40354170-A-G
• MyVariant Identifiers: chr4:g.40356187A>G (hg19) ; chr4:g.40354170A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.40354170A>G , CM000666.2:g.40354170A>G	GRCh38
NC_000004.11:g.40356187A>G , CM000666.1:g.40356187A>G	GRCh37
NC_000004.10:g.40050944A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310169.3:c.1090A>G MANE Select	ENSP00000312663.2:p.Ser364Gly
ENST00000310169.2:c.1090A>G	ENSP00000312663.2:p.Ser364Gly
NM_017581.3:c.1090A>G	NP_060051.2:p.Ser364Gly
NM_017581.4:c.1090A>G MANE Select	NP_060051.2:p.Ser364Gly