Canonical Allele Identifier: CA794799033
Gene: CHRNA9 HGNC NCBI

Linked Data

dbSNP Id: rs1204578800
MyVariant Identifiers: chr4:g.40356418_40356419insC (hg19) chr4:g.40354401_40354402insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354403dup , CM000666.2:g.40354403dup GRCh38
NC_000004.11:g.40356420dup , CM000666.1:g.40356420dup GRCh37
NC_000004.10:g.40051177dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.1323dup MANE Select ENSP00000312663.2:p.Asn442GlnfsTer6
ENST00000310169.2:c.1323dup ENSP00000312663.2:p.Asn442GlnfsTer6
NM_017581.3:c.1323dup NP_060051.2:p.Asn442GlnfsTer6
NM_017581.4:c.1323dup MANE Select NP_060051.2:p.Asn442GlnfsTer6
Search 100 bp 5'
Search 100 bp 3'