Canonical Allele Identifier: CA439141439
Gene: CHRNA9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.40356333G>A (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000310169.3:c.1236G>A MANE Select ENSP00000312663.2:p.Gln412=
ENST00000310169.2:c.1236G>A ENSP00000312663.2:p.Gln412=
NM_017581.3:c.1236G>A NP_060051.2:p.Gln412=
NM_017581.4:c.1236G>A MANE Select NP_060051.2:p.Gln412=