Canonical Allele Identifier: CA439141457
Gene: CHRNA9 HGNC NCBI

Linked Data

dbSNP Id: rs774219510
gnomAD v2: 4-40356342-G-A
gnomAD v4: 4-40354325-G-A
MyVariant Identifiers: chr4:g.40356342G>A (hg19) chr4:g.40354325G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354325G>A , CM000666.2:g.40354325G>A GRCh38
NC_000004.11:g.40356342G>A , CM000666.1:g.40356342G>A GRCh37
NC_000004.10:g.40051099G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000310169.3:c.1245G>A MANE Select ENSP00000312663.2:p.Glu415=
ENST00000310169.2:c.1245G>A ENSP00000312663.2:p.Glu415=
NM_017581.3:c.1245G>A NP_060051.2:p.Glu415=
NM_017581.4:c.1245G>A MANE Select NP_060051.2:p.Glu415=
Search 100 bp 5'
Search 100 bp 3'