Canonical Allele Identifier: CA2142606010

Gene: ESR2

Linked Data

• dbSNP Id: rs2077148690

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.64308968del , CM000676.2:g.64308968del	GRCh38
NC_000014.8:g.64775686del , CM000676.1:g.64775686del	GRCh37
NC_000014.7:g.63845439del	NCBI36
NG_011535.1:g.34587del

Transcript Alleles

HGVS	Amino-acid change
ENST00000358599.9:c.-90-25889del	ENSP00000351412.5:n.-90-25889del
ENST00000554572.5:c.-767-5305del	ENSP00000450699.1:n.-767-5305del
NM_001291712.1:c.-767-5305del	NP_001278641.1:n.-767-5305del
NM_001291723.1:c.-90-25889del	NP_001278652.1:n.-90-25889del
NR_073496.1:n.654-25889del
XM_011536546.1:c.-488+106del	XP_011534848.1:n.-488+106del
XM_017021079.1:c.-90-25889del	XP_016876568.1:n.-90-25889del
XM_017021080.1:c.-90-25889del	XP_016876569.1:n.-90-25889del
XM_017021081.1:c.-90-25889del	XP_016876570.1:n.-90-25889del
XM_017021082.1:c.-90-25889del	XP_016876571.1:n.-90-25889del
XM_017021083.1:c.-90-25889del	XP_016876572.1:n.-90-25889del
XM_017021084.1:c.-90-25889del	XP_016876573.1:n.-90-25889del
NM_001291712.2:c.-767-5305del	NP_001278641.1:n.-767-5305del
NR_073496.2:n.717-25889del