Canonical Allele Identifier: CA749208638

Gene: ETS2

Linked Data

• dbSNP Id: rs1189114581
• gnomAD v3: 21-38823425-T-C
• gnomAD v4: 21-38823425-T-C
• MyVariant Identifiers: chr21:g.40195349T>C (hg19) ; chr21:g.38823425T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.38823425T>C , CM000683.2:g.38823425T>C	GRCh38
NC_000021.8:g.40195349T>C , CM000683.1:g.40195349T>C	GRCh37
NC_000021.7:g.39117219T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360214.8:c.*536T>C	ENSP00000353344.3:n.*536T>C
ENST00000360938.8:c.*536T>C MANE Select	ENSP00000354194.3:n.*536T>C
ENST00000653642.1:c.*536T>C	ENSP00000499315.1:n.*536T>C
ENST00000662305.1:c.*536T>C	ENSP00000499226.1:n.*536T>C
ENST00000666778.1:c.*536T>C	ENSP00000499775.1:n.*536T>C
ENST00000667466.1:c.*536T>C	ENSP00000499540.1:n.*536T>C
ENST00000360214.7:c.*536T>C	ENSP00000353344.3:n.*536T>C
ENST00000360938.7:c.*536T>C	ENSP00000354194.3:n.*536T>C
NM_001256295.1:c.*536T>C	NP_001243224.1:n.*536T>C
NM_005239.5:c.*536T>C	NP_005230.1:n.*536T>C
XM_005260935.1:c.*536T>C	XP_005260992.1:n.*536T>C
XM_017028290.1:c.*536T>C	XP_016883779.1:n.*536T>C
NM_005239.6:c.*536T>C MANE Select	NP_005230.1:n.*536T>C
NM_001256295.2:c.*536T>C	NP_001243224.1:n.*536T>C