LDH info

Canonical Allele Identifier: CA15802837
Gene: ESR2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2987983

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.64296935A>G , CM000676.2:g.64296935A>G GRCh38
NC_000014.8:g.64763653A>G , CM000676.1:g.64763653A>G GRCh37
NC_000014.7:g.63833406A>G NCBI36
NG_011535.1:g.46616T>C

Transcript Alleles

HGVS Amino-acid change
NM_001291712.1:c.-91+598T>C VV NP_001278641.1:p.=
NM_001291723.1:c.-90-13860T>C VV NP_001278652.1:p.=
NR_073496.1:n.654-13860T>C
XM_011536546.1:c.-91+4433T>C XP_011534848.1:p.=
XM_017021079.1:c.-90-13860T>C XP_016876568.1:p.=
XM_017021080.1:c.-90-13860T>C XP_016876569.1:p.=
XM_017021081.1:c.-90-13860T>C XP_016876570.1:p.=
XM_017021082.1:c.-90-13860T>C XP_016876571.1:p.=
XM_017021083.1:c.-90-13860T>C XP_016876572.1:p.=
XM_017021084.1:c.-90-13860T>C XP_016876573.1:p.=
NM_001291712.2:c.-91+598T>C VV NP_001278641.1:p.=
NR_073496.2:n.717-13860T>C
ENST00000358599.9:c.-90-13860T>C ENSP00000351412.5:p.=
ENST00000554572.5:c.-91+598T>C ENSP00000450699.1:p.=