Canonical Allele Identifier: CA356705487
Gene: CHRNA9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.40356131T>G (hg19) chr4:g.40354114T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354114T>G , CM000666.2:g.40354114T>G GRCh38
NC_000004.11:g.40356131T>G , CM000666.1:g.40356131T>G GRCh37
NC_000004.10:g.40050888T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000310169.3:c.1034T>G MANE Select ENSP00000312663.2:p.Met345Arg
ENST00000310169.2:c.1034T>G ENSP00000312663.2:p.Met345Arg
NM_017581.3:c.1034T>G NP_060051.2:p.Met345Arg
NM_017581.4:c.1034T>G MANE Select NP_060051.2:p.Met345Arg
Search 100 bp 5'
Search 100 bp 3'