Canonical Allele Identifier: CA439141164
Gene: CHRNA9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.40356078G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354061G>C , CM000666.2:g.40354061G>C GRCh38
NC_000004.11:g.40356078G>C , CM000666.1:g.40356078G>C GRCh37
NC_000004.10:g.40050835G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.981G>C MANE Select ENSP00000312663.2:p.Gly327=
ENST00000310169.2:c.981G>C ENSP00000312663.2:p.Gly327=
ENST00000509518.1:n.432G>C
NM_017581.3:c.981G>C NP_060051.2:p.Gly327=
NM_017581.4:c.981G>C MANE Select NP_060051.2:p.Gly327=
Search 100 bp 5'
Search 100 bp 3'