Canonical Allele Identifier: CA267922606

Gene: HERC2

Linked Data

• dbSNP Id: rs959174490
• MyVariant Identifiers: chr15:g.28427962A>G (hg19) ; chr15:g.28182816A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28182816A>G , CM000677.2:g.28182816A>G	GRCh38
NC_000015.9:g.28427962A>G , CM000677.1:g.28427962A>G	GRCh37
NC_000015.8:g.26101557A>G	NCBI36
NG_016355.1:g.144334T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.8826-304T>C MANE Select	ENSP00000261609.8:n.8826-304T>C
ENST00000650509.1:c.537-304T>C	ENSP00000496936.1:n.537-304T>C
ENST00000261609.11:c.8826-304T>C	ENSP00000261609.7:n.8826-304T>C
NM_004667.5:c.8826-304T>C	NP_004658.3:n.8826-304T>C
XM_005268276.3:c.8712-304T>C	XP_005268333.1:n.8712-304T>C
XM_005268277.3:c.8712-304T>C	XP_005268334.1:n.8712-304T>C
XM_006720726.2:c.8811-304T>C	XP_006720789.1:n.8811-304T>C
XM_006720727.2:c.8568-304T>C	XP_006720790.1:n.8568-304T>C
XM_011522131.1:c.8343-304T>C	XP_011520433.1:n.8343-304T>C
XM_011522132.1:c.6342-304T>C	XP_011520434.1:n.6342-304T>C
XM_011522133.1:c.5571-304T>C	XP_011520435.1:n.5571-304T>C
XM_011522134.1:c.2943-304T>C	XP_011520436.1:n.2943-304T>C
XR_931930.1:n.8955-304T>C
XM_005268276.5:c.8712-304T>C	XP_005268333.1:n.8712-304T>C
XM_006720726.3:c.8811-304T>C	XP_006720789.1:n.8811-304T>C
XM_006720727.3:c.8568-304T>C	XP_006720790.1:n.8568-304T>C
XM_017022695.1:c.8712-304T>C	XP_016878184.1:n.8712-304T>C
XM_017022696.1:c.8712-304T>C	XP_016878185.1:n.8712-304T>C
XM_017022697.1:c.1992-304T>C	XP_016878186.1:n.1992-304T>C
XM_017022698.1:c.1992-304T>C	XP_016878187.1:n.1992-304T>C
XR_931930.2:n.8956-304T>C
NM_004667.6:c.8826-304T>C MANE Select	NP_004658.3:n.8826-304T>C