Canonical Allele Identifier: CA267946274

Gene: HERC2

Linked Data

• dbSNP Id: rs7495220
• gnomAD v3: 15-28141665-C-G
• gnomAD v4: 15-28141665-C-G
• MyVariant Identifiers: chr15:g.28386811C>G (hg19) ; chr15:g.28141665C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141665C>G , CM000677.2:g.28141665C>G	GRCh38
NC_000015.9:g.28386811C>G , CM000677.1:g.28386811C>G	GRCh37
NC_000015.8:g.26060406C>G	NCBI36
NG_016355.1:g.185485G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11817-35G>C MANE Select	ENSP00000261609.8:n.11817-35G>C
ENST00000650509.1:c.3528-35G>C	ENSP00000496936.1:n.3528-35G>C
ENST00000261609.11:c.11817-35G>C	ENSP00000261609.7:n.11817-35G>C
NM_004667.5:c.11817-35G>C	NP_004658.3:n.11817-35G>C
XM_005268276.3:c.11703-35G>C	XP_005268333.1:n.11703-35G>C
XM_005268277.3:c.11703-35G>C	XP_005268334.1:n.11703-35G>C
XM_006720726.2:c.11802-35G>C	XP_006720789.1:n.11802-35G>C
XM_006720727.2:c.11559-35G>C	XP_006720790.1:n.11559-35G>C
XM_011522131.1:c.11334-35G>C	XP_011520433.1:n.11334-35G>C
XM_011522132.1:c.9333-35G>C	XP_011520434.1:n.9333-35G>C
XM_011522133.1:c.8562-35G>C	XP_011520435.1:n.8562-35G>C
XM_011522134.1:c.5934-35G>C	XP_011520436.1:n.5934-35G>C
XM_005268276.5:c.11703-35G>C	XP_005268333.1:n.11703-35G>C
XM_006720726.3:c.11802-35G>C	XP_006720789.1:n.11802-35G>C
XM_006720727.3:c.11559-35G>C	XP_006720790.1:n.11559-35G>C
XM_017022695.1:c.11703-35G>C	XP_016878184.1:n.11703-35G>C
XM_017022696.1:c.11703-35G>C	XP_016878185.1:n.11703-35G>C
XM_017022697.1:c.4983-35G>C	XP_016878186.1:n.4983-35G>C
XM_017022698.1:c.4983-35G>C	XP_016878187.1:n.4983-35G>C
NM_004667.6:c.11817-35G>C MANE Select	NP_004658.3:n.11817-35G>C