LDH info

Canonical Allele Identifier: CA15814598
Gene: ESR2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1256065

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.64232214G>T , CM000676.2:g.64232214G>T GRCh38
NC_000014.8:g.64698932G>T , CM000676.1:g.64698932G>T GRCh37
NC_000014.7:g.63768685G>T NCBI36
NG_011535.1:g.111337C>A

Transcript Alleles

HGVS Amino-acid change
NM_001040275.1:c.1406+2756C>A VV NP_001035365.1:p.=
NM_001214902.1:c.1406+2756C>A VV NP_001201831.1:p.=
NM_001271876.1:c.1406+2756C>A VV NP_001258805.1:p.=
NM_001291712.1:c.1406+2756C>A VV NP_001278641.1:p.=
NM_001291723.1:c.1406+2756C>A VV NP_001278652.1:p.=
NR_073496.1:n.2010+2756C>A
XM_011536545.1:c.1406+2756C>A XP_011534847.1:p.=
XM_011536546.1:c.*923C>A XP_011534848.1:p.=
XM_017021079.1:c.*923C>A XP_016876568.1:p.=
XM_017021080.1:c.*923C>A XP_016876569.1:p.=
XM_017021081.1:c.*923C>A XP_016876570.1:p.=
XM_017021082.1:c.*923C>A XP_016876571.1:p.=
XM_017021083.1:c.*923C>A XP_016876572.1:p.=
XM_017021084.1:c.1406+2756C>A XP_016876573.1:p.=
XR_001750187.1:n.1842+2756C>A
NM_001291712.2:c.1406+2756C>A VV NP_001278641.1:p.=
NR_073496.2:n.2073+2756C>A
ENST00000344288.10:c.*295+2756C>A ENSP00000345616.6:p.=
ENST00000353772.7:c.1406+2756C>A ENSP00000335551.4:p.=
ENST00000358599.9:c.1406+2756C>A ENSP00000351412.5:p.=
ENST00000553796.5:n.1406+2756C>A ENSP00000452426.1:p.=
ENST00000554572.5:c.1406+2756C>A ENSP00000450699.1:p.=
ENST00000555278.5:n.1406+2756C>A ENSP00000450488.1:p.=
ENST00000556275.5:c.1406+2756C>A ENSP00000452485.2:p.=
ENST00000557772.5:n.4162C>A ENSP00000451582.1:p.=