Canonical Allele Identifier: CA2142558058
Gene: ESR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.64227364T= , CM000676.2:g.64227364T= GRCh38
NC_000014.8:g.64694082T= , CM000676.1:g.64694082T= GRCh37
NC_000014.7:g.63763835T= NCBI36
NG_011535.1:g.116187A=
NG_011756.1:g.379400T=
NG_011756.2:g.470466T=

Transcript Alleles

HGVS Amino-acid Change
NM_001040275.1:c.*169A= NP_001035365.1:n.*169A=
NM_001214902.1:c.*526A= NP_001201831.1:n.*526A=
NM_001291712.1:c.*169A= NP_001278641.1:n.*169A=
NM_001291712.2:c.*169A= NP_001278641.1:n.*169A=
NM_001291723.1:c.*169A= NP_001278652.1:n.*169A=
NR_073496.1:n.2261A=
NR_073496.2:n.2324A=
ENST00000353772.7:c.*169A= ENSP00000335551.4:n.*169A=
ENST00000554572.5:c.*169A= ENSP00000450699.1:n.*169A=
ENST00000556275.5:c.1406+7606A= ENSP00000452485.2:n.1406+7606A=
XM_011536545.1:c.1406+7606A= XP_011534847.1:n.1406+7606A=
XR_001750187.1:n.2093A=