Canonical Allele Identifier: CA345012854

Gene: LEFTY2

Linked Data

• dbSNP Id: rs1189849636
• gnomAD v4: 1-225937520-A-G
• MyVariant Identifiers: chr1:g.226125220A>G (hg19) ; chr1:g.225937520A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.225937520A>G , CM000663.2:g.225937520A>G	GRCh38
NC_000001.10:g.226125220A>G , CM000663.1:g.226125220A>G	GRCh37
NC_000001.9:g.224191843A>G	NCBI36
NG_008118.1:g.8701T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366820.10:c.1022T>C MANE Select	ENSP00000355785.5:p.Val341Ala
ENST00000366820.9:c.1022T>C	ENSP00000355785.5:p.Val341Ala
ENST00000420304.6:c.920T>C	ENSP00000388009.2:p.Val307Ala
ENST00000616737.1:c.1022T>C	ENSP00000484300.1:p.Val341Ala
NM_001172425.1:c.920T>C	NP_001165896.1:p.Val307Ala
NM_003240.3:c.1022T>C	NP_003231.2:p.Val341Ala
NM_001172425.2:c.920T>C	NP_001165896.1:p.Val307Ala
NM_003240.4:c.1022T>C	NP_003231.2:p.Val341Ala
NM_003240.5:c.1022T>C MANE Select	NP_003231.2:p.Val341Ala
NM_001172425.3:c.920T>C	NP_001165896.1:p.Val307Ala