Canonical Allele Identifier: CA356705658
Gene: CHRNA9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354152T>G , CM000666.2:g.40354152T>G GRCh38
NC_000004.11:g.40356169T>G , CM000666.1:g.40356169T>G GRCh37
NC_000004.10:g.40050926T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.1072T>G MANE Select ENSP00000312663.2:p.Cys358Gly
ENST00000310169.2:c.1072T>G ENSP00000312663.2:p.Cys358Gly
NM_017581.3:c.1072T>G NP_060051.2:p.Cys358Gly
NM_017581.4:c.1072T>G MANE Select NP_060051.2:p.Cys358Gly