Canonical Allele Identifier: CA356706842

Gene: CHRNA9

Linked Data

• dbSNP Id: rs1173945176
• gnomAD v2: 4-40356358-T-C
• gnomAD v4: 4-40354341-T-C
• MyVariant Identifiers: chr4:g.40356358T>C (hg19) ; chr4:g.40354341T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.40354341T>C , CM000666.2:g.40354341T>C	GRCh38
NC_000004.11:g.40356358T>C , CM000666.1:g.40356358T>C	GRCh37
NC_000004.10:g.40051115T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310169.3:c.1261T>C MANE Select	ENSP00000312663.2:p.Tyr421His
ENST00000310169.2:c.1261T>C	ENSP00000312663.2:p.Tyr421His
NM_017581.3:c.1261T>C	NP_060051.2:p.Tyr421His
NM_017581.4:c.1261T>C MANE Select	NP_060051.2:p.Tyr421His