Canonical Allele Identifier: CA489234632

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386581C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141435C>G , CM000677.2:g.28141435C>G	GRCh38
NC_000015.9:g.28386581C>G , CM000677.1:g.28386581C>G	GRCh37
NC_000015.8:g.26060176C>G	NCBI36
NG_016355.1:g.185715G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261609.13:c.12012G>C MANE Select	ENSP00000261609.8:p.Gly4004=
ENST00000650509.1:c.3723G>C	ENSP00000496936.1:p.Gly1241=
ENST00000261609.11:c.12012G>C	ENSP00000261609.7:p.Gly4004=
NM_004667.5:c.12012G>C	NP_004658.3:p.Gly4004=
XM_005268276.3:c.11898G>C	XP_005268333.1:p.Gly3966=
XM_005268277.3:c.11898G>C	XP_005268334.1:p.Gly3966=
XM_006720726.2:c.11997G>C	XP_006720789.1:p.Gly3999=
XM_006720727.2:c.11754G>C	XP_006720790.1:p.Gly3918=
XM_011522131.1:c.11529G>C	XP_011520433.1:p.Gly3843=
XM_011522132.1:c.9528G>C	XP_011520434.1:p.Gly3176=
XM_011522133.1:c.8757G>C	XP_011520435.1:p.Gly2919=
XM_011522134.1:c.6129G>C	XP_011520436.1:p.Gly2043=
XM_005268276.5:c.11898G>C	XP_005268333.1:p.Gly3966=
XM_006720726.3:c.11997G>C	XP_006720789.1:p.Gly3999=
XM_006720727.3:c.11754G>C	XP_006720790.1:p.Gly3918=
XM_017022695.1:c.11898G>C	XP_016878184.1:p.Gly3966=
XM_017022696.1:c.11898G>C	XP_016878185.1:p.Gly3966=
XM_017022697.1:c.5178G>C	XP_016878186.1:p.Gly1726=
XM_017022698.1:c.5178G>C	XP_016878187.1:p.Gly1726=
NM_004667.6:c.12012G>C MANE Select	NP_004658.3:p.Gly4004=