Canonical Allele Identifier: CA356707108
Gene: CHRNA9 HGNC NCBI

Linked Data

dbSNP Id: rs1560319689
gnomAD v4: 4-40354371-A-G
MyVariant Identifiers: chr4:g.40356388A>G (hg19) chr4:g.40354371A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354371A>G , CM000666.2:g.40354371A>G GRCh38
NC_000004.11:g.40356388A>G , CM000666.1:g.40356388A>G GRCh37
NC_000004.10:g.40051145A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.1291A>G MANE Select ENSP00000312663.2:p.Ile431Val
ENST00000310169.2:c.1291A>G ENSP00000312663.2:p.Ile431Val
NM_017581.3:c.1291A>G NP_060051.2:p.Ile431Val
NM_017581.4:c.1291A>G MANE Select NP_060051.2:p.Ile431Val
Search 100 bp 5'
Search 100 bp 3'