LDH info

Canonical Allele Identifier: CA16193418
Gene: UNC5C HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10032931

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.95537282T>C , CM000666.2:g.95537282T>C GRCh38
NC_000004.11:g.96458433T>C , CM000666.1:g.96458433T>C GRCh37
NC_000004.10:g.96677456T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_003728.3:c.124+11452A>G VV NP_003719.3:p.=
XM_005263321.2:c.124+11452A>G XP_005263378.1:p.=
XM_005263321.3:c.124+11452A>G XP_005263378.1:p.=
NM_003728.4:c.124+11452A>G VV MANE Preferred NP_003719.3:p.=
ENST00000453304.5:c.124+11452A>G ENSP00000406022.1:p.=
ENST00000504962.1:c.124+11452A>G ENSP00000425117.1:p.=
ENST00000506749.5:c.124+11452A>G ENSP00000426153.1:p.=
ENST00000513796.5:c.124+11452A>G ENSP00000426924.1:p.=