Canonical Allele Identifier: CA2142558203

Gene: ESR2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.64227477C= , CM000676.2:g.64227477C=	GRCh38
NC_000014.8:g.64694195C= , CM000676.1:g.64694195C=	GRCh37
NC_000014.7:g.63763948C=	NCBI36
NG_011535.1:g.116074G=
NG_011756.1:g.379513C=
NG_011756.2:g.470579C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353772.7:c.*56G=	ENSP00000335551.4:n.*56G=
ENST00000358599.9:c.*56G=	ENSP00000351412.5:n.*56G=
ENST00000554572.5:c.*56G=	ENSP00000450699.1:n.*56G=
ENST00000555278.5:c.1859G=	ENSP00000450488.1:n.1859G=
ENST00000556275.5:c.1406+7493G=	ENSP00000452485.2:n.1406+7493G=
NM_001040275.1:c.*56G=	NP_001035365.1:n.*56G=
NM_001214902.1:c.*413G=	NP_001201831.1:n.*413G=
NM_001291712.1:c.*56G=	NP_001278641.1:n.*56G=
NM_001291723.1:c.*56G=	NP_001278652.1:n.*56G=
NR_073496.1:n.2148G=
XM_011536545.1:c.1406+7493G=	XP_011534847.1:n.1406+7493G=
XM_017021084.1:c.*56G=	XP_016876573.1:n.*56G=
XR_001750187.1:n.1980G=
NM_001291712.2:c.*56G=	NP_001278641.1:n.*56G=
NR_073496.2:n.2211G=