Canonical Allele Identifier: CA489235038

Gene: HERC2

Linked Data

• gnomAD v4: 15-28141781-A-G
• MyVariant Identifiers: chr15:g.28386927A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141781A>G , CM000677.2:g.28141781A>G	GRCh38
NC_000015.9:g.28386927A>G , CM000677.1:g.28386927A>G	GRCh37
NC_000015.8:g.26060522A>G	NCBI36
NG_016355.1:g.185369T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11766T>C MANE Select	ENSP00000261609.8:p.His3922=
ENST00000650509.1:c.3477T>C	ENSP00000496936.1:p.His1159=
ENST00000261609.11:c.11766T>C	ENSP00000261609.7:p.His3922=
ENST00000564519.1:n.281T>C
NM_004667.5:c.11766T>C	NP_004658.3:p.His3922=
XM_005268276.3:c.11652T>C	XP_005268333.1:p.His3884=
XM_005268277.3:c.11652T>C	XP_005268334.1:p.His3884=
XM_006720726.2:c.11751T>C	XP_006720789.1:p.His3917=
XM_006720727.2:c.11508T>C	XP_006720790.1:p.His3836=
XM_011522131.1:c.11283T>C	XP_011520433.1:p.His3761=
XM_011522132.1:c.9282T>C	XP_011520434.1:p.His3094=
XM_011522133.1:c.8511T>C	XP_011520435.1:p.His2837=
XM_011522134.1:c.5883T>C	XP_011520436.1:p.His1961=
XM_005268276.5:c.11652T>C	XP_005268333.1:p.His3884=
XM_006720726.3:c.11751T>C	XP_006720789.1:p.His3917=
XM_006720727.3:c.11508T>C	XP_006720790.1:p.His3836=
XM_017022695.1:c.11652T>C	XP_016878184.1:p.His3884=
XM_017022696.1:c.11652T>C	XP_016878185.1:p.His3884=
XM_017022697.1:c.4932T>C	XP_016878186.1:p.His1644=
XM_017022698.1:c.4932T>C	XP_016878187.1:p.His1644=
NM_004667.6:c.11766T>C MANE Select	NP_004658.3:p.His3922=