Canonical Allele Identifier: CA2617675067

Gene: ETV6

Linked Data

• dbSNP Id: rs1331447780
• gnomAD v4: 12-11885904-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11885904C>A , CM000674.2:g.11885904C>A	GRCh38
NC_000012.11:g.12038838C>A , CM000674.1:g.12038838C>A	GRCh37
NC_000012.10:g.11930105C>A	NCBI36
NG_011443.1:g.241051C>A , LRG_609:g.241051C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1153-22C>A MANE Select	ENSP00000379658.3:n.1153-22C>A
ENST00000396373.8:c.1153-22C>A	ENSP00000379658.3:n.1153-22C>A
NM_001987.4:c.1153-22C>A , LRG_609t1:c.1153-22C>A	NP_001978.1:n.1153-22C>A
XM_011520607.1:c.1150-22C>A	XP_011518909.1:n.1150-22C>A
XM_011520608.1:c.1126-22C>A	XP_011518910.1:n.1126-22C>A
XM_011520609.1:c.889-22C>A	XP_011518911.1:n.889-22C>A
XM_011520610.1:c.889-22C>A	XP_011518912.1:n.889-22C>A
XM_011520611.1:c.889-22C>A	XP_011518913.1:n.889-22C>A
XM_011520612.1:c.532-22C>A	XP_011518914.1:n.532-22C>A
XM_011520607.2:c.1150-22C>A	XP_011518909.1:n.1150-22C>A
XM_011520608.2:c.1126-22C>A	XP_011518910.1:n.1126-22C>A
XM_011520609.2:c.889-22C>A	XP_011518911.1:n.889-22C>A
XM_011520611.2:c.889-22C>A	XP_011518913.1:n.889-22C>A
XM_011520612.2:c.532-22C>A	XP_011518914.1:n.532-22C>A
XM_017018990.1:c.1018-22C>A	XP_016874479.1:n.1018-22C>A
XM_017018991.1:c.889-22C>A	XP_016874480.1:n.889-22C>A
NM_001987.5:c.1153-22C>A MANE Select	NP_001978.1:n.1153-22C>A