Canonical Allele Identifier: CA356706094
Gene: CHRNA9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.40356266T>A (hg19) chr4:g.40354249T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354249T>A , CM000666.2:g.40354249T>A GRCh38
NC_000004.11:g.40356266T>A , CM000666.1:g.40356266T>A GRCh37
NC_000004.10:g.40051023T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.1169T>A MANE Select ENSP00000312663.2:p.Leu390His
ENST00000310169.2:c.1169T>A ENSP00000312663.2:p.Leu390His
NM_017581.3:c.1169T>A NP_060051.2:p.Leu390His
NM_017581.4:c.1169T>A MANE Select NP_060051.2:p.Leu390His
Search 100 bp 5'
Search 100 bp 3'