Canonical Allele Identifier: CA2142606032

Gene: ESR2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.64308993A= , CM000676.2:g.64308993A=	GRCh38
NC_000014.8:g.64775711A= , CM000676.1:g.64775711A=	GRCh37
NC_000014.7:g.63845464A=	NCBI36
NG_011535.1:g.34558T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000358599.9:c.-90-25918T=	ENSP00000351412.5:n.-90-25918T=
ENST00000554572.5:c.-767-5334T=	ENSP00000450699.1:n.-767-5334T=
NM_001291712.1:c.-767-5334T=	NP_001278641.1:n.-767-5334T=
NM_001291723.1:c.-90-25918T=	NP_001278652.1:n.-90-25918T=
NR_073496.1:n.654-25918T=
XM_011536546.1:c.-488+77T=	XP_011534848.1:n.-488+77T=
XM_017021079.1:c.-90-25918T=	XP_016876568.1:n.-90-25918T=
XM_017021080.1:c.-90-25918T=	XP_016876569.1:n.-90-25918T=
XM_017021081.1:c.-90-25918T=	XP_016876570.1:n.-90-25918T=
XM_017021082.1:c.-90-25918T=	XP_016876571.1:n.-90-25918T=
XM_017021083.1:c.-90-25918T=	XP_016876572.1:n.-90-25918T=
XM_017021084.1:c.-90-25918T=	XP_016876573.1:n.-90-25918T=
NM_001291712.2:c.-767-5334T=	NP_001278641.1:n.-767-5334T=
NR_073496.2:n.717-25918T=