Canonical Allele Identifier: CA356708270
Gene: CHRNA9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.40356466C>G (hg19) chr4:g.40354449C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354449C>G , CM000666.2:g.40354449C>G GRCh38
NC_000004.11:g.40356466C>G , CM000666.1:g.40356466C>G GRCh37
NC_000004.10:g.40051223C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.1369C>G MANE Select ENSP00000312663.2:p.Arg457Gly
ENST00000310169.2:c.1369C>G ENSP00000312663.2:p.Arg457Gly
NM_017581.3:c.1369C>G NP_060051.2:p.Arg457Gly
NM_017581.4:c.1369C>G MANE Select NP_060051.2:p.Arg457Gly
Search 100 bp 5'
Search 100 bp 3'