Canonical Allele Identifier: CA1452583722
Gene: CHRNA9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354216A= , CM000666.2:g.40354216A= GRCh38
NC_000004.11:g.40356233A= , CM000666.1:g.40356233A= GRCh37
NC_000004.10:g.40050990A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000310169.3:c.1136A= MANE Select ENSP00000312663.2:p.Glu379=
ENST00000310169.2:c.1136A= ENSP00000312663.2:p.Glu379=
NM_017581.3:c.1136A= NP_060051.2:p.Glu379=
NM_017581.4:c.1136A= MANE Select NP_060051.2:p.Glu379=