Canonical Allele Identifier: CA356706218
Gene: CHRNA9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354263G>T , CM000666.2:g.40354263G>T GRCh38
NC_000004.11:g.40356280G>T , CM000666.1:g.40356280G>T GRCh37
NC_000004.10:g.40051037G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.1183G>T MANE Select ENSP00000312663.2:p.Asp395Tyr
ENST00000310169.2:c.1183G>T ENSP00000312663.2:p.Asp395Tyr
NM_017581.3:c.1183G>T NP_060051.2:p.Asp395Tyr
NM_017581.4:c.1183G>T MANE Select NP_060051.2:p.Asp395Tyr