Canonical Allele Identifier: CA1452584841
Gene: CHRNA9 HGNC NCBI

Linked Data

dbSNP Id: rs1712908350
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354613T>C , CM000666.2:g.40354613T>C GRCh38
NC_000004.11:g.40356630T>C , CM000666.1:g.40356630T>C GRCh37
NC_000004.10:g.40051387T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.*93T>C MANE Select ENSP00000312663.2:n.*93T>C
ENST00000310169.2:c.*93T>C ENSP00000312663.2:n.*93T>C
NM_017581.3:c.*93T>C NP_060051.2:n.*93T>C
NM_017581.4:c.*93T>C MANE Select NP_060051.2:n.*93T>C
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