Canonical Allele Identifier: CA384044992

Gene: ETV6

Linked Data

• MyVariant Identifiers: chr12:g.12038941G>C (hg19) ; chr12:g.11886007G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11886007G>C , CM000674.2:g.11886007G>C	GRCh38
NC_000012.11:g.12038941G>C , CM000674.1:g.12038941G>C	GRCh37
NC_000012.10:g.11930208G>C	NCBI36
NG_011443.1:g.241154G>C , LRG_609:g.241154G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1234G>C MANE Select	ENSP00000379658.3:p.Gly412Arg
ENST00000266427.3:c.71G>C
ENST00000396373.8:c.1234G>C	ENSP00000379658.3:p.Gly412Arg
NM_001987.4:c.1234G>C , LRG_609t1:c.1234G>C	NP_001978.1:p.Gly412Arg
XM_011520607.1:c.1231G>C	XP_011518909.1:p.Gly411Arg
XM_011520608.1:c.1207G>C	XP_011518910.1:p.Gly403Arg
XM_011520609.1:c.970G>C	XP_011518911.1:p.Gly324Arg
XM_011520610.1:c.970G>C	XP_011518912.1:p.Gly324Arg
XM_011520611.1:c.970G>C	XP_011518913.1:p.Gly324Arg
XM_011520612.1:c.613G>C	XP_011518914.1:p.Gly205Arg
XM_011520607.2:c.1231G>C	XP_011518909.1:p.Gly411Arg
XM_011520608.2:c.1207G>C	XP_011518910.1:p.Gly403Arg
XM_011520609.2:c.970G>C	XP_011518911.1:p.Gly324Arg
XM_011520611.2:c.970G>C	XP_011518913.1:p.Gly324Arg
XM_011520612.2:c.613G>C	XP_011518914.1:p.Gly205Arg
XM_017018990.1:c.1099G>C	XP_016874479.1:p.Gly367Arg
XM_017018991.1:c.970G>C	XP_016874480.1:p.Gly324Arg
NM_001987.5:c.1234G>C MANE Select	NP_001978.1:p.Gly412Arg