Canonical Allele Identifier: CA1420385

Gene: LEFTY2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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