Canonical Allele Identifier: CA356707532
Gene: CHRNA9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354422T>C , CM000666.2:g.40354422T>C GRCh38
NC_000004.11:g.40356439T>C , CM000666.1:g.40356439T>C GRCh37
NC_000004.10:g.40051196T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000310169.3:c.1342T>C MANE Select ENSP00000312663.2:p.Trp448Arg
ENST00000310169.2:c.1342T>C ENSP00000312663.2:p.Trp448Arg
NM_017581.3:c.1342T>C NP_060051.2:p.Trp448Arg
NM_017581.4:c.1342T>C MANE Select NP_060051.2:p.Trp448Arg