Canonical Allele Identifier: CA267922570

Gene: HERC2

Linked Data

• dbSNP Id: rs956860939
• MyVariant Identifiers: chr15:g.28427884C>A (hg19) ; chr15:g.28182738C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28182738C>A , CM000677.2:g.28182738C>A	GRCh38
NC_000015.9:g.28427884C>A , CM000677.1:g.28427884C>A	GRCh37
NC_000015.8:g.26101479C>A	NCBI36
NG_016355.1:g.144412G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.8826-226G>T MANE Select	ENSP00000261609.8:n.8826-226G>T
ENST00000650509.1:c.537-226G>T	ENSP00000496936.1:n.537-226G>T
ENST00000261609.11:c.8826-226G>T	ENSP00000261609.7:n.8826-226G>T
NM_004667.5:c.8826-226G>T	NP_004658.3:n.8826-226G>T
XM_005268276.3:c.8712-226G>T	XP_005268333.1:n.8712-226G>T
XM_005268277.3:c.8712-226G>T	XP_005268334.1:n.8712-226G>T
XM_006720726.2:c.8811-226G>T	XP_006720789.1:n.8811-226G>T
XM_006720727.2:c.8568-226G>T	XP_006720790.1:n.8568-226G>T
XM_011522131.1:c.8343-226G>T	XP_011520433.1:n.8343-226G>T
XM_011522132.1:c.6342-226G>T	XP_011520434.1:n.6342-226G>T
XM_011522133.1:c.5571-226G>T	XP_011520435.1:n.5571-226G>T
XM_011522134.1:c.2943-226G>T	XP_011520436.1:n.2943-226G>T
XR_931930.1:n.8955-226G>T
XM_005268276.5:c.8712-226G>T	XP_005268333.1:n.8712-226G>T
XM_006720726.3:c.8811-226G>T	XP_006720789.1:n.8811-226G>T
XM_006720727.3:c.8568-226G>T	XP_006720790.1:n.8568-226G>T
XM_017022695.1:c.8712-226G>T	XP_016878184.1:n.8712-226G>T
XM_017022696.1:c.8712-226G>T	XP_016878185.1:n.8712-226G>T
XM_017022697.1:c.1992-226G>T	XP_016878186.1:n.1992-226G>T
XM_017022698.1:c.1992-226G>T	XP_016878187.1:n.1992-226G>T
XR_931930.2:n.8956-226G>T
NM_004667.6:c.8826-226G>T MANE Select	NP_004658.3:n.8826-226G>T