Canonical Allele Identifier: CA1420389

Gene: LEFTY2

Linked Data

• dbSNP Id: rs191981298
• ExAC: 1:226125118 G / T
• gnomAD v2: 1-226125118-G-T
• gnomAD v3: 1-225937418-G-T
• gnomAD v4: 1-225937418-G-T
• MyVariant Identifiers: chr1:g.226125118G>T (hg19) ; chr1:g.225937418G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.225937418G>T , CM000663.2:g.225937418G>T	GRCh38
NC_000001.10:g.226125118G>T , CM000663.1:g.226125118G>T	GRCh37
NC_000001.9:g.224191741G>T	NCBI36
NG_008118.1:g.8803C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366820.10:c.*23C>A MANE Select	ENSP00000355785.5:n.*23C>A
ENST00000366820.9:c.*23C>A	ENSP00000355785.5:n.*23C>A
ENST00000420304.6:c.*23C>A	ENSP00000388009.2:n.*23C>A
ENST00000616737.1:c.*3C>A	ENSP00000484300.1:n.*3C>A
NM_001172425.1:c.*23C>A	NP_001165896.1:n.*23C>A
NM_003240.3:c.*23C>A	NP_003231.2:n.*23C>A
NM_001172425.2:c.*23C>A	NP_001165896.1:n.*23C>A
NM_003240.4:c.*23C>A	NP_003231.2:n.*23C>A
NM_003240.5:c.*23C>A MANE Select	NP_003231.2:n.*23C>A
NM_001172425.3:c.*23C>A	NP_001165896.1:n.*23C>A