Canonical Allele Identifier: CA1452583943
Gene: CHRNA9 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354332T= , CM000666.2:g.40354332T= GRCh38
NC_000004.11:g.40356349T= , CM000666.1:g.40356349T= GRCh37
NC_000004.10:g.40051106T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000310169.3:c.1252T= MANE Select ENSP00000312663.2:p.Cys418=
ENST00000310169.2:c.1252T= ENSP00000312663.2:p.Cys418=
NM_017581.3:c.1252T= NP_060051.2:p.Cys418=
NM_017581.4:c.1252T= MANE Select NP_060051.2:p.Cys418=
Search 100 bp 5'
Search 100 bp 3'