Canonical Allele Identifier: CA2389091551

Gene: ETS2

Linked Data

• dbSNP Id: rs948160013

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.38823851A>C , CM000683.2:g.38823851A>C	GRCh38
NC_000021.8:g.40195775A>C , CM000683.1:g.40195775A>C	GRCh37
NC_000021.7:g.39117645A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360214.8:c.*962A>C	ENSP00000353344.3:n.*962A>C
ENST00000360938.8:c.*962A>C MANE Select	ENSP00000354194.3:n.*962A>C
ENST00000653642.1:c.*962A>C	ENSP00000499315.1:n.*962A>C
ENST00000666778.1:c.*962A>C	ENSP00000499775.1:n.*962A>C
ENST00000667466.1:c.*962A>C	ENSP00000499540.1:n.*962A>C
ENST00000360214.7:c.*962A>C	ENSP00000353344.3:n.*962A>C
ENST00000360938.7:c.*962A>C	ENSP00000354194.3:n.*962A>C
NM_001256295.1:c.*962A>C	NP_001243224.1:n.*962A>C
NM_005239.5:c.*962A>C	NP_005230.1:n.*962A>C
XM_005260935.1:c.*962A>C	XP_005260992.1:n.*962A>C
XM_017028290.1:c.*962A>C	XP_016883779.1:n.*962A>C
NM_005239.6:c.*962A>C MANE Select	NP_005230.1:n.*962A>C
NM_001256295.2:c.*962A>C	NP_001243224.1:n.*962A>C