Canonical Allele Identifier: CA749208850

Gene: ETS2

Linked Data

• dbSNP Id: rs1322708195
• gnomAD v3: 21-38823933-C-T
• gnomAD v4: 21-38823933-C-T
• MyVariant Identifiers: chr21:g.40195857C>T (hg19) ; chr21:g.38823933C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.38823933C>T , CM000683.2:g.38823933C>T	GRCh38
NC_000021.8:g.40195857C>T , CM000683.1:g.40195857C>T	GRCh37
NC_000021.7:g.39117727C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360214.8:c.*1044C>T	ENSP00000353344.3:n.*1044C>T
ENST00000360938.8:c.*1044C>T MANE Select	ENSP00000354194.3:n.*1044C>T
ENST00000653642.1:c.*1044C>T	ENSP00000499315.1:n.*1044C>T
ENST00000666778.1:c.*1044C>T	ENSP00000499775.1:n.*1044C>T
ENST00000667466.1:c.*1044C>T	ENSP00000499540.1:n.*1044C>T
ENST00000360214.7:c.*1044C>T	ENSP00000353344.3:n.*1044C>T
ENST00000360938.7:c.*1044C>T	ENSP00000354194.3:n.*1044C>T
NM_001256295.1:c.*1044C>T	NP_001243224.1:n.*1044C>T
NM_005239.5:c.*1044C>T	NP_005230.1:n.*1044C>T
XM_005260935.1:c.*1044C>T	XP_005260992.1:n.*1044C>T
XM_017028290.1:c.*1044C>T	XP_016883779.1:n.*1044C>T
NM_005239.6:c.*1044C>T MANE Select	NP_005230.1:n.*1044C>T
NM_001256295.2:c.*1044C>T	NP_001243224.1:n.*1044C>T