Canonical Allele Identifier: CA1022324294

Gene: ETS2

Linked Data

• dbSNP Id: rs2060967953
• gnomAD v3: 21-38823788-T-A
• gnomAD v4: 21-38823788-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.38823788T>A , CM000683.2:g.38823788T>A	GRCh38
NC_000021.8:g.40195712T>A , CM000683.1:g.40195712T>A	GRCh37
NC_000021.7:g.39117582T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360214.8:c.*899T>A	ENSP00000353344.3:n.*899T>A
ENST00000360938.8:c.*899T>A MANE Select	ENSP00000354194.3:n.*899T>A
ENST00000653642.1:c.*899T>A	ENSP00000499315.1:n.*899T>A
ENST00000666778.1:c.*899T>A	ENSP00000499775.1:n.*899T>A
ENST00000667466.1:c.*899T>A	ENSP00000499540.1:n.*899T>A
ENST00000360214.7:c.*899T>A	ENSP00000353344.3:n.*899T>A
ENST00000360938.7:c.*899T>A	ENSP00000354194.3:n.*899T>A
NM_001256295.1:c.*899T>A	NP_001243224.1:n.*899T>A
NM_005239.5:c.*899T>A	NP_005230.1:n.*899T>A
XM_005260935.1:c.*899T>A	XP_005260992.1:n.*899T>A
XM_017028290.1:c.*899T>A	XP_016883779.1:n.*899T>A
NM_005239.6:c.*899T>A MANE Select	NP_005230.1:n.*899T>A
NM_001256295.2:c.*899T>A	NP_001243224.1:n.*899T>A