Canonical Allele Identifier: CA262511767

Gene: ESR2

Linked Data

• dbSNP Id: rs1035036902
• gnomAD v3: 14-64296731-A-G
• gnomAD v4: 14-64296731-A-G
• MyVariant Identifiers: chr14:g.64763449A>G (hg19) ; chr14:g.64296731A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.64296731A>G , CM000676.2:g.64296731A>G	GRCh38
NC_000014.8:g.64763449A>G , CM000676.1:g.64763449A>G	GRCh37
NC_000014.7:g.63833202A>G	NCBI36
NG_011535.1:g.46820T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358599.9:c.-90-13656T>C	ENSP00000351412.5:n.-90-13656T>C
ENST00000554572.5:c.-91+802T>C	ENSP00000450699.1:n.-91+802T>C
NM_001291712.1:c.-91+802T>C	NP_001278641.1:n.-91+802T>C
NM_001291723.1:c.-90-13656T>C	NP_001278652.1:n.-90-13656T>C
NR_073496.1:n.654-13656T>C
XM_011536546.1:c.-91+4637T>C	XP_011534848.1:n.-91+4637T>C
XM_017021079.1:c.-90-13656T>C	XP_016876568.1:n.-90-13656T>C
XM_017021080.1:c.-90-13656T>C	XP_016876569.1:n.-90-13656T>C
XM_017021081.1:c.-90-13656T>C	XP_016876570.1:n.-90-13656T>C
XM_017021082.1:c.-90-13656T>C	XP_016876571.1:n.-90-13656T>C
XM_017021083.1:c.-90-13656T>C	XP_016876572.1:n.-90-13656T>C
XM_017021084.1:c.-90-13656T>C	XP_016876573.1:n.-90-13656T>C
NM_001291712.2:c.-91+802T>C	NP_001278641.1:n.-91+802T>C
NR_073496.2:n.717-13656T>C