Canonical Allele Identifier: CA14074460
Gene: HERC2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs7170852

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.28182840T>A , CM000677.2:g.28182840T>A GRCh38
NC_000015.9:g.28427986T>A , CM000677.1:g.28427986T>A GRCh37
NC_000015.8:g.26101581T>A NCBI36
NG_016355.1:g.144310A>T

Transcript Alleles

HGVS Amino-acid change
NM_004667.5:c.8826-328A>T VV NP_004658.3:p.=
XM_005268276.3:c.8712-328A>T XP_005268333.1:p.=
XM_005268277.3:c.8712-328A>T XP_005268334.1:p.=
XM_006720726.2:c.8811-328A>T XP_006720789.1:p.=
XM_006720727.2:c.8568-328A>T XP_006720790.1:p.=
XM_011522131.1:c.8343-328A>T XP_011520433.1:p.=
XM_011522132.1:c.6342-328A>T XP_011520434.1:p.=
XM_011522133.1:c.5571-328A>T XP_011520435.1:p.=
XM_011522134.1:c.2943-328A>T XP_011520436.1:p.=
XR_931930.1:n.8955-328A>T
XM_005268276.5:c.8712-328A>T XP_005268333.1:p.=
XM_006720726.3:c.8811-328A>T XP_006720789.1:p.=
XM_006720727.3:c.8568-328A>T XP_006720790.1:p.=
XM_017022695.1:c.8712-328A>T XP_016878184.1:p.=
XM_017022696.1:c.8712-328A>T XP_016878185.1:p.=
XM_017022697.1:c.1992-328A>T XP_016878186.1:p.=
XM_017022698.1:c.1992-328A>T XP_016878187.1:p.=
XR_931930.2:n.8956-328A>T
ENST00000261609.11:c.8826-328A>T ENSP00000261609.7:p.=