Canonical Allele Identifier: CA1452584656
Gene: CHRNA9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354498T= , CM000666.2:g.40354498T= GRCh38
NC_000004.11:g.40356515T= , CM000666.1:g.40356515T= GRCh37
NC_000004.10:g.40051272T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.1418T= MANE Select ENSP00000312663.2:p.Leu473=
ENST00000310169.2:c.1418T= ENSP00000312663.2:p.Leu473=
NM_017581.3:c.1418T= NP_060051.2:p.Leu473=
NM_017581.4:c.1418T= MANE Select NP_060051.2:p.Leu473=
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