Canonical Allele Identifier: CA2142599816
Gene: ESR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.64297006A= , CM000676.2:g.64297006A= GRCh38
NC_000014.8:g.64763724A= , CM000676.1:g.64763724A= GRCh37
NC_000014.7:g.63833477A= NCBI36
NG_011535.1:g.46545T=

Transcript Alleles

HGVS Amino-acid change
ENST00000358599.9:c.-90-13931T= ENSP00000351412.5:n.-90-13931T=
ENST00000554572.5:c.-91+527T= ENSP00000450699.1:n.-91+527T=
NM_001291712.1:c.-91+527T= NP_001278641.1:n.-91+527T=
NM_001291723.1:c.-90-13931T= NP_001278652.1:n.-90-13931T=
NR_073496.1:n.654-13931T=
XM_011536546.1:c.-91+4362T= XP_011534848.1:n.-91+4362T=
XM_017021079.1:c.-90-13931T= XP_016876568.1:n.-90-13931T=
XM_017021080.1:c.-90-13931T= XP_016876569.1:n.-90-13931T=
XM_017021081.1:c.-90-13931T= XP_016876570.1:n.-90-13931T=
XM_017021082.1:c.-90-13931T= XP_016876571.1:n.-90-13931T=
XM_017021083.1:c.-90-13931T= XP_016876572.1:n.-90-13931T=
XM_017021084.1:c.-90-13931T= XP_016876573.1:n.-90-13931T=
NM_001291712.2:c.-91+527T= NP_001278641.1:n.-91+527T=
NR_073496.2:n.717-13931T=