LDH info

Canonical Allele Identifier: CA12819766
Gene: TNFRSF11B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1032128

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118939534G>A , CM000670.2:g.118939534G>A GRCh38
NC_000008.10:g.119951773G>A , CM000670.1:g.119951773G>A GRCh37
NC_000008.9:g.120020954G>A NCBI36
NG_012202.1:g.17611C>T

Transcript Alleles

HGVS Amino-acid change
NM_002546.3:c.31-6234C>T VV NP_002537.3:p.=
NM_002546.4:c.31-6234C>T VV MANE Preferred NP_002537.3:p.=
ENST00000297350.8:c.31-6234C>T ENSP00000297350.4:p.=
ENST00000517352.1:c.31-6234C>T ENSP00000427924.1:p.=