Canonical Allele Identifier: CA1420384

Gene: LEFTY2

Linked Data

• dbSNP Id: rs199559277
• ExAC: 1:226125103 C / T
• gnomAD v2: 1-226125103-C-T
• gnomAD v3: 1-225937403-C-T
• gnomAD v4: 1-225937403-C-T
• MyVariant Identifiers: chr1:g.226125103C>T (hg19) ; chr1:g.225937403C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.225937403C>T , CM000663.2:g.225937403C>T	GRCh38
NC_000001.10:g.226125103C>T , CM000663.1:g.226125103C>T	GRCh37
NC_000001.9:g.224191726C>T	NCBI36
NG_008118.1:g.8818G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366820.10:c.*38G>A MANE Select	ENSP00000355785.5:n.*38G>A
ENST00000366820.9:c.*38G>A	ENSP00000355785.5:n.*38G>A
ENST00000420304.6:c.*38G>A	ENSP00000388009.2:n.*38G>A
ENST00000616737.1:c.*18G>A	ENSP00000484300.1:n.*18G>A
NM_001172425.1:c.*38G>A	NP_001165896.1:n.*38G>A
NM_003240.3:c.*38G>A	NP_003231.2:n.*38G>A
NM_001172425.2:c.*38G>A	NP_001165896.1:n.*38G>A
NM_003240.4:c.*38G>A	NP_003231.2:n.*38G>A
NM_003240.5:c.*38G>A MANE Select	NP_003231.2:n.*38G>A
NM_001172425.3:c.*38G>A	NP_001165896.1:n.*38G>A