Canonical Allele Identifier: CA2670423992
Gene: CHRNA9 HGNC NCBI

Linked Data

gnomAD v4: 4-40354527-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354527A>T , CM000666.2:g.40354527A>T GRCh38
NC_000004.11:g.40356544A>T , CM000666.1:g.40356544A>T GRCh37
NC_000004.10:g.40051301A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.*7A>T MANE Select ENSP00000312663.2:n.*7A>T
ENST00000310169.2:c.*7A>T ENSP00000312663.2:n.*7A>T
NM_017581.3:c.*7A>T NP_060051.2:n.*7A>T
NM_017581.4:c.*7A>T MANE Select NP_060051.2:n.*7A>T
Search 100 bp 5'
Search 100 bp 3'