Canonical Allele Identifier: CA345012435
Gene: LEFTY2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.226125122C>G (hg19) chr1:g.225937422C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.225937422C>G , CM000663.2:g.225937422C>G GRCh38
NC_000001.10:g.226125122C>G , CM000663.1:g.226125122C>G GRCh37
NC_000001.9:g.224191745C>G NCBI36
NG_008118.1:g.8799G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000366820.10:c.*19G>C MANE Select ENSP00000355785.5:n.*19G>C
ENST00000366820.9:c.*19G>C ENSP00000355785.5:n.*19G>C
ENST00000420304.6:c.*19G>C ENSP00000388009.2:n.*19G>C
ENST00000616737.1:c.1118G>C ENSP00000484300.1:p.Ter373Ser
NM_001172425.1:c.*19G>C NP_001165896.1:n.*19G>C
NM_003240.3:c.*19G>C NP_003231.2:n.*19G>C
NM_001172425.2:c.*19G>C NP_001165896.1:n.*19G>C
NM_003240.4:c.*19G>C NP_003231.2:n.*19G>C
NM_003240.5:c.*19G>C MANE Select NP_003231.2:n.*19G>C
NM_001172425.3:c.*19G>C NP_001165896.1:n.*19G>C
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