Canonical Allele Identifier: CA356706451

Gene: CHRNA9

Linked Data

• dbSNP Id: rs1261838941
• gnomAD v2: 4-40356319-G-A
• gnomAD v4: 4-40354302-G-A
• MyVariant Identifiers: chr4:g.40356319G>A (hg19) ; chr4:g.40354302G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.40354302G>A , CM000666.2:g.40354302G>A	GRCh38
NC_000004.11:g.40356319G>A , CM000666.1:g.40356319G>A	GRCh37
NC_000004.10:g.40051076G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310169.3:c.1222G>A MANE Select	ENSP00000312663.2:p.Gly408Ser
ENST00000310169.2:c.1222G>A	ENSP00000312663.2:p.Gly408Ser
NM_017581.3:c.1222G>A	NP_060051.2:p.Gly408Ser
NM_017581.4:c.1222G>A MANE Select	NP_060051.2:p.Gly408Ser