Canonical Allele Identifier: CA2898125
Gene: CHRNA9 HGNC NCBI

Linked Data

dbSNP Id: rs761815662
gnomAD v2: 4-40356139-G-T
gnomAD v3: 4-40354122-G-T
gnomAD v4: 4-40354122-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354122G>T , CM000666.2:g.40354122G>T GRCh38
NC_000004.11:g.40356139G>T , CM000666.1:g.40356139G>T GRCh37
NC_000004.10:g.40050896G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.1042G>T MANE Select ENSP00000312663.2:p.Val348Phe
ENST00000310169.2:c.1042G>T ENSP00000312663.2:p.Val348Phe
NM_017581.3:c.1042G>T NP_060051.2:p.Val348Phe
NM_017581.4:c.1042G>T MANE Select NP_060051.2:p.Val348Phe