Canonical Allele Identifier: CA550745440
Gene: CHRNA9 HGNC NCBI

Linked Data

dbSNP Id: rs1362922180
gnomAD v2: 4-40356637-G-C
gnomAD v3: 4-40354620-G-C
gnomAD v4: 4-40354620-G-C
MyVariant Identifiers: chr4:g.40356637G>C (hg19) chr4:g.40354620G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354620G>C , CM000666.2:g.40354620G>C GRCh38
NC_000004.11:g.40356637G>C , CM000666.1:g.40356637G>C GRCh37
NC_000004.10:g.40051394G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.*100G>C MANE Select ENSP00000312663.2:n.*100G>C
ENST00000310169.2:c.*100G>C ENSP00000312663.2:n.*100G>C
NM_017581.3:c.*100G>C NP_060051.2:n.*100G>C
NM_017581.4:c.*100G>C MANE Select NP_060051.2:n.*100G>C
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