Canonical Allele Identifier: CA637810182

Gene: ETS2

Linked Data

• dbSNP Id: rs1425974379
• gnomAD v2: 21-40194162-T-C
• gnomAD v3: 21-38822238-T-C
• gnomAD v4: 21-38822238-T-C
• MyVariant Identifiers: chr21:g.40194162T>C (hg19) ; chr21:g.38822238T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.38822238T>C , CM000683.2:g.38822238T>C	GRCh38
NC_000021.8:g.40194162T>C , CM000683.1:g.40194162T>C	GRCh37
NC_000021.7:g.39116032T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000360214.8:c.1195-436T>C	ENSP00000353344.3:n.1195-436T>C
ENST00000360938.8:c.1195-436T>C MANE Select	ENSP00000354194.3:n.1195-436T>C
ENST00000653642.1:c.1195-436T>C	ENSP00000499315.1:n.1195-436T>C
ENST00000662305.1:c.1195-436T>C	ENSP00000499226.1:n.1195-436T>C
ENST00000666778.1:c.1195-436T>C	ENSP00000499775.1:n.1195-436T>C
ENST00000667466.1:c.1300-436T>C	ENSP00000499540.1:n.1300-436T>C
ENST00000360214.7:c.1195-436T>C	ENSP00000353344.3:n.1195-436T>C
ENST00000360938.7:c.1195-436T>C	ENSP00000354194.3:n.1195-436T>C
NM_001256295.1:c.1615-436T>C	NP_001243224.1:n.1615-436T>C
NM_005239.5:c.1195-436T>C	NP_005230.1:n.1195-436T>C
XM_005260935.1:c.1195-436T>C	XP_005260992.1:n.1195-436T>C
XM_017028290.1:c.1195-436T>C	XP_016883779.1:n.1195-436T>C
NM_005239.6:c.1195-436T>C MANE Select	NP_005230.1:n.1195-436T>C
NM_001256295.2:c.1615-436T>C	NP_001243224.1:n.1615-436T>C