LDH info

Canonical Allele Identifier: CA253858
Gene: FLNB HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 6402
dbSNP Id: rs28937587

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.58109627G>C , CM000665.2:g.58109627G>C GRCh38
NC_000003.11:g.58095354G>C , CM000665.1:g.58095354G>C GRCh37
NC_000003.10:g.58070394G>C NCBI36
NG_012801.1:g.106228G>C

Transcript Alleles

HGVS Amino-acid change
NM_001164317.1:c.2251G>C VV NP_001157789.1:p.Gly751Arg
NM_001164318.1:c.2251G>C VV NP_001157790.1:p.Gly751Arg
NM_001164319.1:c.2251G>C VV NP_001157791.1:p.Gly751Arg
NM_001457.3:c.2251G>C VV NP_001448.2:p.Gly751Arg
XM_005264977.1:c.2251G>C XP_005265034.1:p.Gly751Arg
XM_005264978.1:c.2251G>C XP_005265035.1:p.Gly751Arg
XM_005264981.1:c.2251G>C XP_005265038.1:p.Gly751Arg
XR_940396.1:n.2396G>C
XM_005264978.2:c.2251G>C XP_005265035.1:p.Gly751Arg
XR_001740065.1:n.2396G>C
XR_940396.2:n.2396G>C
ENST00000295956.8:c.2251G>C ENSP00000295956.4:p.Gly751Arg
ENST00000358537.7:c.2251G>C ENSP00000351339.3:p.Gly751Arg
ENST00000429972.6:c.2251G>C ENSP00000415599.2:p.Gly751Arg
ENST00000490882.5:c.2251G>C ENSP00000420213.1:p.Gly751Arg
ENST00000493452.5:c.1744G>C ENSP00000418510.1:p.Gly582Arg