LDH info

Canonical Allele Identifier: CA15428568
Gene: FKBP5 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1360780

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35639794T>C , CM000668.2:g.35639794T>C GRCh38
NC_000006.11:g.35607571T>C , CM000668.1:g.35607571T>C GRCh37
NC_000006.10:g.35715549T>C NCBI36
NG_012645.2:g.93790A>G

Transcript Alleles

HGVS Amino-acid change
NM_001145775.2:c.106-2636A>G VV NP_001139247.1:p.=
NM_001145776.1:c.106-2636A>G VV NP_001139248.1:p.=
NM_001145777.1:c.106-2636A>G VV NP_001139249.1:p.=
NM_004117.3:c.106-2636A>G VV NP_004108.1:p.=
XR_926743.1:n.287+5974T>C
XR_002956345.1:n.1483-9556T>C
NM_001145775.3:c.106-2636A>G VV NP_001139247.1:p.=
NM_001145776.2:c.106-2636A>G VV NP_001139248.1:p.=
NM_001145777.2:c.106-2636A>G VV NP_001139249.1:p.=
NM_004117.4:c.106-2636A>G VV MANE Preferred NP_004108.1:p.=
ENST00000357266.8:c.106-2636A>G ENSP00000349811.3:p.=
ENST00000536438.5:c.106-2636A>G ENSP00000444810.1:p.=
ENST00000539068.5:c.106-2636A>G ENSP00000441205.1:p.=
ENST00000542713.1:c.106-2636A>G ENSP00000442340.1:p.=