Canonical Allele Identifier: CA356705573
Gene: CHRNA9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.40356151T>C (hg19) chr4:g.40354134T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354134T>C , CM000666.2:g.40354134T>C GRCh38
NC_000004.11:g.40356151T>C , CM000666.1:g.40356151T>C GRCh37
NC_000004.10:g.40050908T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000310169.3:c.1054T>C MANE Select ENSP00000312663.2:p.Tyr352His
ENST00000310169.2:c.1054T>C ENSP00000312663.2:p.Tyr352His
NM_017581.3:c.1054T>C NP_060051.2:p.Tyr352His
NM_017581.4:c.1054T>C MANE Select NP_060051.2:p.Tyr352His
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