Canonical Allele Identifier: CA1452584185
Gene: CHRNA9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354427G= , CM000666.2:g.40354427G= GRCh38
NC_000004.11:g.40356444G= , CM000666.1:g.40356444G= GRCh37
NC_000004.10:g.40051201G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000310169.3:c.1347G= MANE Select ENSP00000312663.2:p.Lys449=
ENST00000310169.2:c.1347G= ENSP00000312663.2:p.Lys449=
NM_017581.3:c.1347G= NP_060051.2:p.Lys449=
NM_017581.4:c.1347G= MANE Select NP_060051.2:p.Lys449=