Canonical Allele Identifier: CA261856752
Gene: ESR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1259581
ClinVar RCV Id: RCV001673957
dbSNP Id: rs10140457

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.64249975A>C , CM000676.2:g.64249975A>C GRCh38
NC_000014.8:g.64716693A>C , CM000676.1:g.64716693A>C GRCh37
NC_000014.7:g.63786446A>C NCBI36
NG_011535.1:g.93576T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000341099.6:c.1092-296T>G MANE Select ENSP00000343925.4:n.1092-296T>G
ENST00000267525.10:c.952+10474T>G ENSP00000267525.6:n.952+10474T>G
ENST00000341099.5:c.1092-296T>G ENSP00000343925.4:n.1092-296T>G
ENST00000344288.10:c.953-296T>G ENSP00000345616.6:n.953-296T>G
ENST00000353772.7:c.1092-296T>G ENSP00000335551.4:n.1092-296T>G
ENST00000358599.9:c.1092-296T>G ENSP00000351412.5:n.1092-296T>G
ENST00000553796.5:c.1092-296T>G ENSP00000452426.1:n.1092-296T>G
ENST00000554520.1:n.780+10474T>G
ENST00000554572.5:c.1092-296T>G ENSP00000450699.1:n.1092-296T>G
ENST00000555278.5:c.1092-296T>G ENSP00000450488.1:n.1092-296T>G
ENST00000555483.5:n.827-296T>G
ENST00000555783.1:n.218+7251T>G
ENST00000556275.5:c.1092-296T>G ENSP00000452485.2:n.1092-296T>G
ENST00000557772.5:c.1092-296T>G ENSP00000451582.1:n.1092-296T>G
NM_001040275.1:c.1092-296T>G NP_001035365.1:n.1092-296T>G
NM_001214902.1:c.1092-296T>G NP_001201831.1:n.1092-296T>G
NM_001271876.1:c.1092-296T>G NP_001258805.1:n.1092-296T>G
NM_001271877.1:c.952+10474T>G NP_001258806.1:n.952+10474T>G
NM_001291712.1:c.1092-296T>G NP_001278641.1:n.1092-296T>G
NM_001291723.1:c.1092-296T>G NP_001278652.1:n.1092-296T>G
NM_001437.2:c.1092-296T>G NP_001428.1:n.1092-296T>G
NR_073496.1:n.1696-296T>G
NR_073497.1:n.1060-296T>G
XM_011536545.1:c.1092-296T>G XP_011534847.1:n.1092-296T>G
XM_011536546.1:c.1092-296T>G XP_011534848.1:n.1092-296T>G
XM_017021079.1:c.1092-296T>G XP_016876568.1:n.1092-296T>G
XM_017021080.1:c.1092-296T>G XP_016876569.1:n.1092-296T>G
XM_017021081.1:c.1092-296T>G XP_016876570.1:n.1092-296T>G
XM_017021082.1:c.1092-296T>G XP_016876571.1:n.1092-296T>G
XM_017021083.1:c.1092-296T>G XP_016876572.1:n.1092-296T>G
XM_017021084.1:c.1092-296T>G XP_016876573.1:n.1092-296T>G
XR_001750187.1:n.1528-296T>G
NM_001291712.2:c.1092-296T>G NP_001278641.1:n.1092-296T>G
NR_073496.2:n.1759-296T>G
NM_001437.3:c.1092-296T>G MANE Select NP_001428.1:n.1092-296T>G