Canonical Allele Identifier: CA423731156
Gene: LEFTY2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.226125303C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.225937603C>G , CM000663.2:g.225937603C>G GRCh38
NC_000001.10:g.226125303C>G , CM000663.1:g.226125303C>G GRCh37
NC_000001.9:g.224191926C>G NCBI36
NG_008118.1:g.8618G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000366820.10:c.939G>C MANE Select ENSP00000355785.5:p.Pro313=
ENST00000366820.9:c.939G>C ENSP00000355785.5:p.Pro313=
ENST00000420304.6:c.837G>C ENSP00000388009.2:p.Pro279=
ENST00000616737.1:c.939G>C ENSP00000484300.1:p.Pro313=
NM_001172425.1:c.837G>C NP_001165896.1:p.Pro279=
NM_003240.3:c.939G>C NP_003231.2:p.Pro313=
NM_001172425.2:c.837G>C NP_001165896.1:p.Pro279=
NM_003240.4:c.939G>C NP_003231.2:p.Pro313=
NM_003240.5:c.939G>C MANE Select NP_003231.2:p.Pro313=
NM_001172425.3:c.837G>C NP_001165896.1:p.Pro279=