Canonical Allele Identifier: CA478767205

Gene: ETV6

Linked Data

• gnomAD v4: 12-11885958-C-G
• MyVariant Identifiers: chr12:g.12038892C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11885958C>G , CM000674.2:g.11885958C>G	GRCh38
NC_000012.11:g.12038892C>G , CM000674.1:g.12038892C>G	GRCh37
NC_000012.10:g.11930159C>G	NCBI36
NG_011443.1:g.241105C>G , LRG_609:g.241105C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1185C>G MANE Select	ENSP00000379658.3:p.Ser395=
ENST00000266427.3:c.22C>G
ENST00000396373.8:c.1185C>G	ENSP00000379658.3:p.Ser395=
NM_001987.4:c.1185C>G , LRG_609t1:c.1185C>G	NP_001978.1:p.Ser395=
XM_011520607.1:c.1182C>G	XP_011518909.1:p.Ser394=
XM_011520608.1:c.1158C>G	XP_011518910.1:p.Ser386=
XM_011520609.1:c.921C>G	XP_011518911.1:p.Ser307=
XM_011520610.1:c.921C>G	XP_011518912.1:p.Ser307=
XM_011520611.1:c.921C>G	XP_011518913.1:p.Ser307=
XM_011520612.1:c.564C>G	XP_011518914.1:p.Ser188=
XM_011520607.2:c.1182C>G	XP_011518909.1:p.Ser394=
XM_011520608.2:c.1158C>G	XP_011518910.1:p.Ser386=
XM_011520609.2:c.921C>G	XP_011518911.1:p.Ser307=
XM_011520611.2:c.921C>G	XP_011518913.1:p.Ser307=
XM_011520612.2:c.564C>G	XP_011518914.1:p.Ser188=
XM_017018990.1:c.1050C>G	XP_016874479.1:p.Ser350=
XM_017018991.1:c.921C>G	XP_016874480.1:p.Ser307=
NM_001987.5:c.1185C>G MANE Select	NP_001978.1:p.Ser395=