Canonical Allele Identifier: CA489234779

Gene: HERC2

Linked Data

• gnomAD v4: 15-28141563-T-G
• MyVariant Identifiers: chr15:g.28386709T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141563T>G , CM000677.2:g.28141563T>G	GRCh38
NC_000015.9:g.28386709T>G , CM000677.1:g.28386709T>G	GRCh37
NC_000015.8:g.26060304T>G	NCBI36
NG_016355.1:g.185587A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11884A>C MANE Select	ENSP00000261609.8:p.Arg3962=
ENST00000650509.1:c.3595A>C	ENSP00000496936.1:p.Arg1199=
ENST00000261609.11:c.11884A>C	ENSP00000261609.7:p.Arg3962=
NM_004667.5:c.11884A>C	NP_004658.3:p.Arg3962=
XM_005268276.3:c.11770A>C	XP_005268333.1:p.Arg3924=
XM_005268277.3:c.11770A>C	XP_005268334.1:p.Arg3924=
XM_006720726.2:c.11869A>C	XP_006720789.1:p.Arg3957=
XM_006720727.2:c.11626A>C	XP_006720790.1:p.Arg3876=
XM_011522131.1:c.11401A>C	XP_011520433.1:p.Arg3801=
XM_011522132.1:c.9400A>C	XP_011520434.1:p.Arg3134=
XM_011522133.1:c.8629A>C	XP_011520435.1:p.Arg2877=
XM_011522134.1:c.6001A>C	XP_011520436.1:p.Arg2001=
XM_005268276.5:c.11770A>C	XP_005268333.1:p.Arg3924=
XM_006720726.3:c.11869A>C	XP_006720789.1:p.Arg3957=
XM_006720727.3:c.11626A>C	XP_006720790.1:p.Arg3876=
XM_017022695.1:c.11770A>C	XP_016878184.1:p.Arg3924=
XM_017022696.1:c.11770A>C	XP_016878185.1:p.Arg3924=
XM_017022697.1:c.5050A>C	XP_016878186.1:p.Arg1684=
XM_017022698.1:c.5050A>C	XP_016878187.1:p.Arg1684=
NM_004667.6:c.11884A>C MANE Select	NP_004658.3:p.Arg3962=