Canonical Allele Identifier: CA38551153

Gene: LEFTY2

Linked Data

• dbSNP Id: rs1040981250
• gnomAD v2: 1-226125322-T-C
• gnomAD v3: 1-225937622-T-C
• gnomAD v4: 1-225937622-T-C
• MyVariant Identifiers: chr1:g.226125322T>C (hg19) ; chr1:g.225937622T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.225937622T>C , CM000663.2:g.225937622T>C	GRCh38
NC_000001.10:g.226125322T>C , CM000663.1:g.226125322T>C	GRCh37
NC_000001.9:g.224191945T>C	NCBI36
NG_008118.1:g.8599A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000366820.10:c.920A>G MANE Select	ENSP00000355785.5:p.Asn307Ser
ENST00000366820.9:c.920A>G	ENSP00000355785.5:p.Asn307Ser
ENST00000420304.6:c.818A>G	ENSP00000388009.2:p.Asn273Ser
ENST00000616737.1:c.920A>G	ENSP00000484300.1:p.Asn307Ser
NM_001172425.1:c.818A>G	NP_001165896.1:p.Asn273Ser
NM_003240.3:c.920A>G	NP_003231.2:p.Asn307Ser
NM_001172425.2:c.818A>G	NP_001165896.1:p.Asn273Ser
NM_003240.4:c.920A>G	NP_003231.2:p.Asn307Ser
NM_003240.5:c.920A>G MANE Select	NP_003231.2:p.Asn307Ser
NM_001172425.3:c.818A>G	NP_001165896.1:p.Asn273Ser