Canonical Allele Identifier: CA345012449

Gene: LEFTY2

Linked Data

• dbSNP Id: rs1424257215
• gnomAD v2: 1-226125125-T-C
• gnomAD v3: 1-225937425-T-C
• gnomAD v4: 1-225937425-T-C
• MyVariant Identifiers: chr1:g.226125125T>C (hg19) ; chr1:g.225937425T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.225937425T>C , CM000663.2:g.225937425T>C	GRCh38
NC_000001.10:g.226125125T>C , CM000663.1:g.226125125T>C	GRCh37
NC_000001.9:g.224191748T>C	NCBI36
NG_008118.1:g.8796A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000366820.10:c.*16A>G MANE Select	ENSP00000355785.5:n.*16A>G
ENST00000366820.9:c.*16A>G	ENSP00000355785.5:n.*16A>G
ENST00000420304.6:c.*16A>G	ENSP00000388009.2:n.*16A>G
ENST00000616737.1:c.1115A>G	ENSP00000484300.1:p.His372Arg
NM_001172425.1:c.*16A>G	NP_001165896.1:n.*16A>G
NM_003240.3:c.*16A>G	NP_003231.2:n.*16A>G
NM_001172425.2:c.*16A>G	NP_001165896.1:n.*16A>G
NM_003240.4:c.*16A>G	NP_003231.2:n.*16A>G
NM_003240.5:c.*16A>G MANE Select	NP_003231.2:n.*16A>G
NM_001172425.3:c.*16A>G	NP_001165896.1:n.*16A>G