LDH info

Canonical Allele Identifier: CA16066877
Gene: IL6R HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs12730935

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154447416G>A , CM000663.2:g.154447416G>A GRCh38
NC_000001.10:g.154419892G>A , CM000663.1:g.154419892G>A GRCh37
NC_000001.9:g.152686516G>A NCBI36
NG_012087.1:g.47224G>A

Transcript Alleles

HGVS Amino-acid change
NM_000565.3:c.950-709G>A VV NP_000556.1:p.=
NM_181359.2:c.950-709G>A VV NP_852004.1:p.=
XM_005245139.1:c.808-709G>A XP_005245196.1:p.=
XM_005245140.1:c.808-709G>A XP_005245197.1:p.=
XM_006711298.1:c.998-709G>A XP_006711361.1:p.=
XM_006711299.2:c.998-709G>A XP_006711362.1:p.=
XM_005245139.2:c.808-709G>A XP_005245196.1:p.=
XM_005245140.3:c.808-709G>A XP_005245197.1:p.=
XM_006711298.2:c.998-709G>A XP_006711361.1:p.=
XM_006711299.4:c.998-709G>A XP_006711362.1:p.=
XM_017001199.2:c.998-709G>A XP_016856688.1:p.=
XM_017001200.2:c.950-709G>A XP_016856689.1:p.=
XM_017001201.2:c.808-709G>A XP_016856690.1:p.=
NM_000565.4:c.950-709G>A VV MANE Preferred NP_000556.1:p.=
NM_181359.3:c.950-709G>A VV NP_852004.1:p.=
ENST00000344086.8:c.950-709G>A ENSP00000340589.4:p.=
ENST00000368485.7:c.950-709G>A ENSP00000357470.3:p.=
ENST00000476006.5:n.766-709G>A
ENST00000507256.1:n.148-709G>A
ENST00000515190.1:n.358-709G>A