Canonical Allele Identifier: CA356705544
Gene: CHRNA9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.40356145T>A (hg19) chr4:g.40354128T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354128T>A , CM000666.2:g.40354128T>A GRCh38
NC_000004.11:g.40356145T>A , CM000666.1:g.40356145T>A GRCh37
NC_000004.10:g.40050902T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000310169.3:c.1048T>A MANE Select ENSP00000312663.2:p.Phe350Ile
ENST00000310169.2:c.1048T>A ENSP00000312663.2:p.Phe350Ile
NM_017581.3:c.1048T>A NP_060051.2:p.Phe350Ile
NM_017581.4:c.1048T>A MANE Select NP_060051.2:p.Phe350Ile
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