Canonical Allele Identifier: CA2142599813
Gene: ESR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.64297003C= , CM000676.2:g.64297003C= GRCh38
NC_000014.8:g.64763721C= , CM000676.1:g.64763721C= GRCh37
NC_000014.7:g.63833474C= NCBI36
NG_011535.1:g.46548G=

Transcript Alleles

HGVS Amino-acid change
ENST00000358599.9:c.-90-13928G= ENSP00000351412.5:n.-90-13928G=
ENST00000554572.5:c.-91+530G= ENSP00000450699.1:n.-91+530G=
NM_001291712.1:c.-91+530G= NP_001278641.1:n.-91+530G=
NM_001291723.1:c.-90-13928G= NP_001278652.1:n.-90-13928G=
NR_073496.1:n.654-13928G=
XM_011536546.1:c.-91+4365G= XP_011534848.1:n.-91+4365G=
XM_017021079.1:c.-90-13928G= XP_016876568.1:n.-90-13928G=
XM_017021080.1:c.-90-13928G= XP_016876569.1:n.-90-13928G=
XM_017021081.1:c.-90-13928G= XP_016876570.1:n.-90-13928G=
XM_017021082.1:c.-90-13928G= XP_016876571.1:n.-90-13928G=
XM_017021083.1:c.-90-13928G= XP_016876572.1:n.-90-13928G=
XM_017021084.1:c.-90-13928G= XP_016876573.1:n.-90-13928G=
NM_001291712.2:c.-91+530G= NP_001278641.1:n.-91+530G=
NR_073496.2:n.717-13928G=