Canonical Allele Identifier: CA749207882

Gene: ETS2

Linked Data

• dbSNP Id: rs916231075
• gnomAD v3: 21-38822222-G-C
• gnomAD v4: 21-38822222-G-C
• MyVariant Identifiers: chr21:g.40194146G>C (hg19) ; chr21:g.38822222G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.38822222G>C , CM000683.2:g.38822222G>C	GRCh38
NC_000021.8:g.40194146G>C , CM000683.1:g.40194146G>C	GRCh37
NC_000021.7:g.39116016G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360214.8:c.1195-452G>C	ENSP00000353344.3:n.1195-452G>C
ENST00000360938.8:c.1195-452G>C MANE Select	ENSP00000354194.3:n.1195-452G>C
ENST00000653642.1:c.1195-452G>C	ENSP00000499315.1:n.1195-452G>C
ENST00000662305.1:c.1195-452G>C	ENSP00000499226.1:n.1195-452G>C
ENST00000666778.1:c.1195-452G>C	ENSP00000499775.1:n.1195-452G>C
ENST00000667466.1:c.1300-452G>C	ENSP00000499540.1:n.1300-452G>C
ENST00000360214.7:c.1195-452G>C	ENSP00000353344.3:n.1195-452G>C
ENST00000360938.7:c.1195-452G>C	ENSP00000354194.3:n.1195-452G>C
NM_001256295.1:c.1615-452G>C	NP_001243224.1:n.1615-452G>C
NM_005239.5:c.1195-452G>C	NP_005230.1:n.1195-452G>C
XM_005260935.1:c.1195-452G>C	XP_005260992.1:n.1195-452G>C
XM_017028290.1:c.1195-452G>C	XP_016883779.1:n.1195-452G>C
NM_005239.6:c.1195-452G>C MANE Select	NP_005230.1:n.1195-452G>C
NM_001256295.2:c.1615-452G>C	NP_001243224.1:n.1615-452G>C