Canonical Allele Identifier: CA2898184
Gene: CHRNA9 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10009228

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354405A>G , CM000666.2:g.40354405A>G GRCh38
NC_000004.11:g.40356422A>G , CM000666.1:g.40356422A>G GRCh37
NC_000004.10:g.40051179A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_017581.3:c.1325A>G VV NP_060051.2:p.Asn442Ser
NM_017581.4:c.1325A>G VV MANE Preferred NP_060051.2:p.Asn442Ser
ENST00000310169.2:c.1325A>G ENSP00000312663.2:p.Asn442Ser