Canonical Allele Identifier: CA2578072178
Gene: CHRNA9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354606T>C , CM000666.2:g.40354606T>C GRCh38
NC_000004.11:g.40356623T>C , CM000666.1:g.40356623T>C GRCh37
NC_000004.10:g.40051380T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.*86T>C MANE Select ENSP00000312663.2:n.*86T>C
ENST00000310169.2:c.*86T>C ENSP00000312663.2:n.*86T>C
NM_017581.3:c.*86T>C NP_060051.2:n.*86T>C
NM_017581.4:c.*86T>C MANE Select NP_060051.2:n.*86T>C
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