Canonical Allele Identifier: CA118943
Gene: LEFTY2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 7639
ClinVar RCV Id: RCV000008078
dbSNP Id: rs121909125

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.225937602G>A , CM000663.2:g.225937602G>A GRCh38
NC_000001.10:g.226125302G>A , CM000663.1:g.226125302G>A GRCh37
NC_000001.9:g.224191925G>A NCBI36
NG_008118.1:g.8619C>T

Transcript Alleles

HGVS Amino-acid change
NM_001172425.1:c.838C>T VV NP_001165896.1:p.Arg280Ter
NM_003240.3:c.940C>T VV NP_003231.2:p.Arg314Ter
NM_001172425.2:c.838C>T VV
NM_003240.4:c.940C>T VV
ENST00000366820.9:c.940C>T ENSP00000355785.5:p.Arg314Ter
ENST00000420304.6:c.838C>T ENSP00000388009.2:p.Arg280Ter
ENST00000616737.1:c.940C>T ENSP00000484300.1:p.Arg314Ter