Canonical Allele Identifier: CA2817885426

Gene: ETS2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.38823791T>C , CM000683.2:g.38823791T>C	GRCh38
NC_000021.8:g.40195715T>C , CM000683.1:g.40195715T>C	GRCh37
NC_000021.7:g.39117585T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000360214.8:c.*902T>C	ENSP00000353344.3:n.*902T>C
ENST00000360938.8:c.*902T>C MANE Select	ENSP00000354194.3:n.*902T>C
ENST00000653642.1:c.*902T>C	ENSP00000499315.1:n.*902T>C
ENST00000666778.1:c.*902T>C	ENSP00000499775.1:n.*902T>C
ENST00000667466.1:c.*902T>C	ENSP00000499540.1:n.*902T>C
ENST00000360214.7:c.*902T>C	ENSP00000353344.3:n.*902T>C
ENST00000360938.7:c.*902T>C	ENSP00000354194.3:n.*902T>C
NM_001256295.1:c.*902T>C	NP_001243224.1:n.*902T>C
NM_005239.5:c.*902T>C	NP_005230.1:n.*902T>C
XM_005260935.1:c.*902T>C	XP_005260992.1:n.*902T>C
XM_017028290.1:c.*902T>C	XP_016883779.1:n.*902T>C
NM_005239.6:c.*902T>C MANE Select	NP_005230.1:n.*902T>C
NM_001256295.2:c.*902T>C	NP_001243224.1:n.*902T>C