Canonical Allele Identifier: CA439141275
Gene: CHRNA9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.40356159G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354142G>T , CM000666.2:g.40354142G>T GRCh38
NC_000004.11:g.40356159G>T , CM000666.1:g.40356159G>T GRCh37
NC_000004.10:g.40050916G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.1062G>T MANE Select ENSP00000312663.2:p.Val354=
ENST00000310169.2:c.1062G>T ENSP00000312663.2:p.Val354=
NM_017581.3:c.1062G>T NP_060051.2:p.Val354=
NM_017581.4:c.1062G>T MANE Select NP_060051.2:p.Val354=