Canonical Allele Identifier: CA438955552
Gene: CHRNA9 HGNC NCBI

Linked Data

gnomAD v4: 4-40354433-G-A
MyVariant Identifiers: chr4:g.40356450G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354433G>A , CM000666.2:g.40354433G>A GRCh38
NC_000004.11:g.40356450G>A , CM000666.1:g.40356450G>A GRCh37
NC_000004.10:g.40051207G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000310169.3:c.1353G>A MANE Select ENSP00000312663.2:p.Val451=
ENST00000310169.2:c.1353G>A ENSP00000312663.2:p.Val451=
NM_017581.3:c.1353G>A NP_060051.2:p.Val451=
NM_017581.4:c.1353G>A MANE Select NP_060051.2:p.Val451=
Search 100 bp 5'
Search 100 bp 3'