LDH info

Canonical Allele Identifier: CA120084
Gene: VANGL2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 9053
ClinVar RCV Id: RCV000009620
dbSNP Id: rs267607168

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160425122T>C , CM000663.2:g.160425122T>C GRCh38
NC_000001.10:g.160394912T>C , CM000663.1:g.160394912T>C GRCh37
NC_000001.9:g.158661536T>C NCBI36
NG_023420.1:g.29549T>C

Transcript Alleles

HGVS Amino-acid change
NM_020335.2:c.1310T>C VV NP_065068.1:p.Phe437Ser
XM_005245357.1:c.1310T>C XP_005245414.1:p.Phe437Ser
XM_011509804.1:c.1310T>C XP_011508106.1:p.Phe437Ser
NM_020335.3:c.1310T>C VV MANE Preferred NP_065068.1:p.Phe437Ser
ENST00000368061.2:c.1310T>C ENSP00000357040.2:p.Phe437Ser