Canonical Allele Identifier: CA2142615629
Community Standard Title: NC_000014.9:g.64338283A=
Gene: ESR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.64338283A= , CM000676.2:g.64338283A= GRCh38
NC_000014.8:g.64805001A= , CM000676.1:g.64805001A= GRCh37
NC_000014.7:g.63874754A= NCBI36
NG_011535.1:g.5268T=

Transcript Alleles

HGVS Amino-acid Change
NM_001291712.1:c.-1461T= NP_001278641.1:n.-1461T=
NM_001291712.2:c.-1461T= NP_001278641.1:n.-1461T=
NM_001291723.1:c.-476T= NP_001278652.1:n.-476T=
NR_073496.1:n.268T=
NR_073496.2:n.331T=
XM_017021079.1:c.-784T= XP_016876568.1:n.-784T=
XM_017021080.1:c.-1593T= XP_016876569.1:n.-1593T=
XM_017021081.1:c.-689T= XP_016876570.1:n.-689T=
XM_017021084.1:c.-784T= XP_016876573.1:n.-784T=