Canonical Allele Identifier: CA1022323853

Gene: ETS2

Linked Data

• dbSNP Id: rs183216601
• gnomAD v3: 21-38822248-G-T
• gnomAD v4: 21-38822248-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.38822248G>T , CM000683.2:g.38822248G>T	GRCh38
NC_000021.8:g.40194172G>T , CM000683.1:g.40194172G>T	GRCh37
NC_000021.7:g.39116042G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000360214.8:c.1195-426G>T	ENSP00000353344.3:n.1195-426G>T
ENST00000360938.8:c.1195-426G>T MANE Select	ENSP00000354194.3:n.1195-426G>T
ENST00000653642.1:c.1195-426G>T	ENSP00000499315.1:n.1195-426G>T
ENST00000662305.1:c.1195-426G>T	ENSP00000499226.1:n.1195-426G>T
ENST00000666778.1:c.1195-426G>T	ENSP00000499775.1:n.1195-426G>T
ENST00000667466.1:c.1300-426G>T	ENSP00000499540.1:n.1300-426G>T
ENST00000360214.7:c.1195-426G>T	ENSP00000353344.3:n.1195-426G>T
ENST00000360938.7:c.1195-426G>T	ENSP00000354194.3:n.1195-426G>T
NM_001256295.1:c.1615-426G>T	NP_001243224.1:n.1615-426G>T
NM_005239.5:c.1195-426G>T	NP_005230.1:n.1195-426G>T
XM_005260935.1:c.1195-426G>T	XP_005260992.1:n.1195-426G>T
XM_017028290.1:c.1195-426G>T	XP_016883779.1:n.1195-426G>T
NM_005239.6:c.1195-426G>T MANE Select	NP_005230.1:n.1195-426G>T
NM_001256295.2:c.1615-426G>T	NP_001243224.1:n.1615-426G>T