Canonical Allele Identifier: CA473229142
Gene: FAR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.13750213C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.13728666C>G , CM000673.2:g.13728666C>G GRCh38
NC_000011.9:g.13750213C>G , CM000673.1:g.13750213C>G GRCh37
NC_000011.8:g.13706789C>G NCBI36
NG_041826.1:g.65008C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703358.1:c.*265C>G ENSP00000515269.1:n.*265C>G
ENST00000354817.8:c.1440C>G MANE Select ENSP00000346874.3:p.Arg480=
ENST00000354817.7:c.1440C>G ENSP00000346874.3:p.Arg480=
ENST00000532502.1:c.312C>G ENSP00000434624.1:p.Arg104=
NM_032228.5:c.1440C>G NP_115604.1:p.Arg480=
XM_011520400.1:c.1449C>G XP_011518702.1:p.Arg483=
XM_011520401.1:c.1272C>G XP_011518703.1:p.Arg424=
XM_011520400.2:c.1449C>G XP_011518702.1:p.Arg483=
NM_032228.6:c.1440C>G MANE Select NP_115604.1:p.Arg480=