LDH info

Canonical Allele Identifier: CA15271790
Gene: FLNB HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs939882

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.58097719G>A , CM000665.2:g.58097719G>A GRCh38
NC_000003.11:g.58083446G>A , CM000665.1:g.58083446G>A GRCh37
NC_000003.10:g.58058486G>A NCBI36
NG_012801.1:g.94320G>A

Transcript Alleles

HGVS Amino-acid change
NM_001164317.1:c.985-96G>A VV NP_001157789.1:p.=
NM_001164318.1:c.985-96G>A VV NP_001157790.1:p.=
NM_001164319.1:c.985-96G>A VV NP_001157791.1:p.=
NM_001457.3:c.985-96G>A VV NP_001448.2:p.=
XM_005264977.1:c.985-96G>A XP_005265034.1:p.=
XM_005264978.1:c.985-96G>A XP_005265035.1:p.=
XM_005264981.1:c.985-96G>A XP_005265038.1:p.=
XR_940396.1:n.1130-96G>A
XM_005264978.2:c.985-96G>A XP_005265035.1:p.=
XR_001740065.1:n.1130-96G>A
XR_940396.2:n.1130-96G>A
ENST00000295956.8:c.985-96G>A ENSP00000295956.4:p.=
ENST00000358537.7:c.985-96G>A ENSP00000351339.3:p.=
ENST00000429972.6:c.985-96G>A ENSP00000415599.2:p.=
ENST00000490882.5:c.985-96G>A ENSP00000420213.1:p.=
ENST00000493452.5:c.478-96G>A ENSP00000418510.1:p.=