Canonical Allele Identifier: CA423731169
Gene: LEFTY2 HGNC NCBI

Linked Data

dbSNP Id: rs1672186008
MyVariant Identifiers: chr1:g.226125324G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.225937624G>A , CM000663.2:g.225937624G>A GRCh38
NC_000001.10:g.226125324G>A , CM000663.1:g.226125324G>A GRCh37
NC_000001.9:g.224191947G>A NCBI36
NG_008118.1:g.8597C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000366820.10:c.918C>T MANE Select ENSP00000355785.5:p.Phe306=
ENST00000366820.9:c.918C>T ENSP00000355785.5:p.Phe306=
ENST00000420304.6:c.816C>T ENSP00000388009.2:p.Phe272=
ENST00000616737.1:c.918C>T ENSP00000484300.1:p.Phe306=
NM_001172425.1:c.816C>T NP_001165896.1:p.Phe272=
NM_003240.3:c.918C>T NP_003231.2:p.Phe306=
NM_001172425.2:c.816C>T NP_001165896.1:p.Phe272=
NM_003240.4:c.918C>T NP_003231.2:p.Phe306=
NM_003240.5:c.918C>T MANE Select NP_003231.2:p.Phe306=
NM_001172425.3:c.816C>T NP_001165896.1:p.Phe272=