Canonical Allele Identifier: CA423731031

Gene: LEFTY2

Linked Data

• dbSNP Id: rs1249174715
• gnomAD v2: 1-226125111-G-A
• gnomAD v3: 1-225937411-G-A
• gnomAD v4: 1-225937411-G-A
• MyVariant Identifiers: chr1:g.226125111G>A (hg19) ; chr1:g.225937411G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.225937411G>A , CM000663.2:g.225937411G>A	GRCh38
NC_000001.10:g.226125111G>A , CM000663.1:g.226125111G>A	GRCh37
NC_000001.9:g.224191734G>A	NCBI36
NG_008118.1:g.8810C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366820.10:c.*30C>T MANE Select	ENSP00000355785.5:n.*30C>T
ENST00000366820.9:c.*30C>T	ENSP00000355785.5:n.*30C>T
ENST00000420304.6:c.*30C>T	ENSP00000388009.2:n.*30C>T
ENST00000616737.1:c.*10C>T	ENSP00000484300.1:n.*10C>T
NM_001172425.1:c.*30C>T	NP_001165896.1:n.*30C>T
NM_003240.3:c.*30C>T	NP_003231.2:n.*30C>T
NM_001172425.2:c.*30C>T	NP_001165896.1:n.*30C>T
NM_003240.4:c.*30C>T	NP_003231.2:n.*30C>T
NM_003240.5:c.*30C>T MANE Select	NP_003231.2:n.*30C>T
NM_001172425.3:c.*30C>T	NP_001165896.1:n.*30C>T