Canonical Allele Identifier: CA16491917
Gene: ESR2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10144225

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.64238276A>G , CM000676.2:g.64238276A>G GRCh38
NC_000014.8:g.64704994A>G , CM000676.1:g.64704994A>G GRCh37
NC_000014.7:g.63774747A>G NCBI36
NG_011535.1:g.105275T>C

Transcript Alleles

HGVS Amino-acid change
NM_001040275.1:c.1226-3126T>C VV NP_001035365.1:p.=
NM_001214902.1:c.1226-3126T>C VV NP_001201831.1:p.=
NM_001271876.1:c.1226-3126T>C VV NP_001258805.1:p.=
NM_001271877.1:c.953-3126T>C VV NP_001258806.1:p.=
NM_001291712.1:c.1226-3126T>C VV NP_001278641.1:p.=
NM_001291723.1:c.1226-3126T>C VV NP_001278652.1:p.=
NM_001437.2:c.1226-3126T>C VV NP_001428.1:p.=
NR_073496.1:n.1830-3126T>C
NR_073497.1:n.1194-3126T>C
XM_011536545.1:c.1226-3126T>C XP_011534847.1:p.=
XM_011536546.1:c.1226-3126T>C XP_011534848.1:p.=
XM_017021079.1:c.1226-3126T>C XP_016876568.1:p.=
XM_017021080.1:c.1226-3126T>C XP_016876569.1:p.=
XM_017021081.1:c.1226-3126T>C XP_016876570.1:p.=
XM_017021082.1:c.1226-3126T>C XP_016876571.1:p.=
XM_017021083.1:c.1226-3126T>C XP_016876572.1:p.=
XM_017021084.1:c.1226-3126T>C XP_016876573.1:p.=
XR_001750187.1:n.1662-3126T>C
ENST00000267525.10:c.953-3126T>C ENSP00000267525.6:p.=
ENST00000341099.5:c.1226-3126T>C ENSP00000343925.4:p.=
ENST00000344288.10:c.*115-3126T>C ENSP00000345616.6:p.=
ENST00000353772.7:c.1226-3126T>C ENSP00000335551.4:p.=
ENST00000358599.9:c.1226-3126T>C ENSP00000351412.5:p.=
ENST00000553796.5:n.1226-3126T>C ENSP00000452426.1:p.=
ENST00000554520.1:n.781-3126T>C
ENST00000554572.5:c.1226-3126T>C ENSP00000450699.1:p.=
ENST00000555278.5:n.1226-3126T>C ENSP00000450488.1:p.=
ENST00000555483.5:n.961-3126T>C
ENST00000555783.1:n.219-3126T>C
ENST00000556275.5:c.1226-3126T>C ENSP00000452485.2:p.=
ENST00000557772.5:n.1226-3126T>C ENSP00000451582.1:p.=