Canonical Allele Identifier: CA356706581

Gene: CHRNA9

Linked Data

• dbSNP Id: rs1712890755
• gnomAD v3: 4-40354316-G-T
• gnomAD v4: 4-40354316-G-T
• MyVariant Identifiers: chr4:g.40356333G>T (hg19) ; chr4:g.40354316G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.40354316G>T , CM000666.2:g.40354316G>T	GRCh38
NC_000004.11:g.40356333G>T , CM000666.1:g.40356333G>T	GRCh37
NC_000004.10:g.40051090G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000310169.3:c.1236G>T MANE Select	ENSP00000312663.2:p.Gln412His
ENST00000310169.2:c.1236G>T	ENSP00000312663.2:p.Gln412His
NM_017581.3:c.1236G>T	NP_060051.2:p.Gln412His
NM_017581.4:c.1236G>T MANE Select	NP_060051.2:p.Gln412His