Canonical Allele Identifier: CA439141568
Gene: CHRNA9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.40356405A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354388A>G , CM000666.2:g.40354388A>G GRCh38
NC_000004.11:g.40356405A>G , CM000666.1:g.40356405A>G GRCh37
NC_000004.10:g.40051162A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.1308A>G MANE Select ENSP00000312663.2:p.Lys436=
ENST00000310169.2:c.1308A>G ENSP00000312663.2:p.Lys436=
NM_017581.3:c.1308A>G NP_060051.2:p.Lys436=
NM_017581.4:c.1308A>G MANE Select NP_060051.2:p.Lys436=
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