Canonical Allele Identifier: CA356708157
Gene: CHRNA9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.40356454A>G (hg19) chr4:g.40354437A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354437A>G , CM000666.2:g.40354437A>G GRCh38
NC_000004.11:g.40356454A>G , CM000666.1:g.40356454A>G GRCh37
NC_000004.10:g.40051211A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000310169.3:c.1357A>G MANE Select ENSP00000312663.2:p.Lys453Glu
ENST00000310169.2:c.1357A>G ENSP00000312663.2:p.Lys453Glu
NM_017581.3:c.1357A>G NP_060051.2:p.Lys453Glu
NM_017581.4:c.1357A>G MANE Select NP_060051.2:p.Lys453Glu
Search 100 bp 5'
Search 100 bp 3'