Canonical Allele Identifier: CA384044904

Gene: ETV6

Linked Data

• MyVariant Identifiers: chr12:g.12038905C>T (hg19) ; chr12:g.11885971C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11885971C>T , CM000674.2:g.11885971C>T	GRCh38
NC_000012.11:g.12038905C>T , CM000674.1:g.12038905C>T	GRCh37
NC_000012.10:g.11930172C>T	NCBI36
NG_011443.1:g.241118C>T , LRG_609:g.241118C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1198C>T MANE Select	ENSP00000379658.3:p.His400Tyr
ENST00000266427.3:c.35C>T
ENST00000396373.8:c.1198C>T	ENSP00000379658.3:p.His400Tyr
NM_001987.4:c.1198C>T , LRG_609t1:c.1198C>T	NP_001978.1:p.His400Tyr
XM_011520607.1:c.1195C>T	XP_011518909.1:p.His399Tyr
XM_011520608.1:c.1171C>T	XP_011518910.1:p.His391Tyr
XM_011520609.1:c.934C>T	XP_011518911.1:p.His312Tyr
XM_011520610.1:c.934C>T	XP_011518912.1:p.His312Tyr
XM_011520611.1:c.934C>T	XP_011518913.1:p.His312Tyr
XM_011520612.1:c.577C>T	XP_011518914.1:p.His193Tyr
XM_011520607.2:c.1195C>T	XP_011518909.1:p.His399Tyr
XM_011520608.2:c.1171C>T	XP_011518910.1:p.His391Tyr
XM_011520609.2:c.934C>T	XP_011518911.1:p.His312Tyr
XM_011520611.2:c.934C>T	XP_011518913.1:p.His312Tyr
XM_011520612.2:c.577C>T	XP_011518914.1:p.His193Tyr
XM_017018990.1:c.1063C>T	XP_016874479.1:p.His355Tyr
XM_017018991.1:c.934C>T	XP_016874480.1:p.His312Tyr
NM_001987.5:c.1198C>T MANE Select	NP_001978.1:p.His400Tyr