Canonical Allele Identifier: CA964011370
Gene: ESR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.64308978T>A , CM000676.2:g.64308978T>A GRCh38
NC_000014.8:g.64775696T>A , CM000676.1:g.64775696T>A GRCh37
NC_000014.7:g.63845449T>A NCBI36
NG_011535.1:g.34573A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000358599.9:c.-90-25903A>T ENSP00000351412.5:n.-90-25903A>T
ENST00000554572.5:c.-767-5319A>T ENSP00000450699.1:n.-767-5319A>T
NM_001291712.1:c.-767-5319A>T NP_001278641.1:n.-767-5319A>T
NM_001291723.1:c.-90-25903A>T NP_001278652.1:n.-90-25903A>T
NR_073496.1:n.654-25903A>T
XM_011536546.1:c.-488+92A>T XP_011534848.1:n.-488+92A>T
XM_017021079.1:c.-90-25903A>T XP_016876568.1:n.-90-25903A>T
XM_017021080.1:c.-90-25903A>T XP_016876569.1:n.-90-25903A>T
XM_017021081.1:c.-90-25903A>T XP_016876570.1:n.-90-25903A>T
XM_017021082.1:c.-90-25903A>T XP_016876571.1:n.-90-25903A>T
XM_017021083.1:c.-90-25903A>T XP_016876572.1:n.-90-25903A>T
XM_017021084.1:c.-90-25903A>T XP_016876573.1:n.-90-25903A>T
NM_001291712.2:c.-767-5319A>T NP_001278641.1:n.-767-5319A>T
NR_073496.2:n.717-25903A>T