Canonical Allele Identifier: CA7439631
Gene: HERC2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1129038

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.28111713C>T , CM000677.2:g.28111713C>T GRCh38
NC_000015.9:g.28356859C>T , CM000677.1:g.28356859C>T GRCh37
NC_000015.8:g.26030454C>T NCBI36
NG_016355.1:g.215437G>A

Transcript Alleles

HGVS Amino-acid change
NM_004667.5:c.*50G>A VV NP_004658.3:p.=
XM_005268276.3:c.*50G>A XP_005268333.1:p.=
XM_005268277.3:c.*50G>A XP_005268334.1:p.=
XM_006720726.2:c.*50G>A XP_006720789.1:p.=
XM_006720727.2:c.*50G>A XP_006720790.1:p.=
XM_011522131.1:c.*50G>A XP_011520433.1:p.=
XM_011522132.1:c.*50G>A XP_011520434.1:p.=
XM_011522133.1:c.*50G>A XP_011520435.1:p.=
XM_011522134.1:c.*50G>A XP_011520436.1:p.=
XM_005268276.5:c.*50G>A XP_005268333.1:p.=
XM_006720726.3:c.*50G>A XP_006720789.1:p.=
XM_006720727.3:c.*50G>A XP_006720790.1:p.=
XM_017022695.1:c.*50G>A XP_016878184.1:p.=
XM_017022696.1:c.*50G>A XP_016878185.1:p.=
XM_017022697.1:c.*50G>A XP_016878186.1:p.=
XM_017022698.1:c.*50G>A XP_016878187.1:p.=
ENST00000261609.11:c.*50G>A ENSP00000261609.7:p.=
ENST00000566635.5:n.1680G>A