LDH info

Canonical Allele Identifier: CA16379761
Gene: CELF2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11256676

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.10559897A>G , CM000672.2:g.10559897A>G GRCh38
NC_000010.10:g.10601860A>G , CM000672.1:g.10601860A>G GRCh37
NC_000010.9:g.10641866A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001326317.1:c.-95+97311A>G VV NP_001313246.1:p.=
NM_001326318.1:c.-95+97311A>G VV NP_001313247.1:p.=
NM_001326319.1:c.-133+97311A>G VV NP_001313248.1:p.=
NM_001326320.1:c.-189+97311A>G VV NP_001313249.1:p.=
NM_001326321.1:c.-95+97311A>G VV NP_001313250.1:p.=
NM_001326323.1:c.-189+97311A>G VV NP_001313252.1:p.=
XM_017015557.1:c.-273+97311A>G XP_016871046.1:p.=
XM_017015568.2:c.-627+97311A>G XP_016871057.1:p.=