Canonical Allele Identifier: CA1452584146
Gene: CHRNA9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354410A= , CM000666.2:g.40354410A= GRCh38
NC_000004.11:g.40356427A= , CM000666.1:g.40356427A= GRCh37
NC_000004.10:g.40051184A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000310169.3:c.1330A= MANE Select ENSP00000312663.2:p.Lys444=
ENST00000310169.2:c.1330A= ENSP00000312663.2:p.Lys444=
NM_017581.3:c.1330A= NP_060051.2:p.Lys444=
NM_017581.4:c.1330A= MANE Select NP_060051.2:p.Lys444=