Canonical Allele Identifier: CA1452583982
Gene: CHRNA9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354364T= , CM000666.2:g.40354364T= GRCh38
NC_000004.11:g.40356381T= , CM000666.1:g.40356381T= GRCh37
NC_000004.10:g.40051138T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.1284T= MANE Select ENSP00000312663.2:p.Ile428=
ENST00000310169.2:c.1284T= ENSP00000312663.2:p.Ile428=
NM_017581.3:c.1284T= NP_060051.2:p.Ile428=
NM_017581.4:c.1284T= MANE Select NP_060051.2:p.Ile428=
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