Canonical Allele Identifier: CA267922587

Gene: HERC2

Linked Data

• dbSNP Id: rs961143071
• MyVariant Identifiers: chr15:g.28427932T>C (hg19) ; chr15:g.28182786T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28182786T>C , CM000677.2:g.28182786T>C	GRCh38
NC_000015.9:g.28427932T>C , CM000677.1:g.28427932T>C	GRCh37
NC_000015.8:g.26101527T>C	NCBI36
NG_016355.1:g.144364A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261609.13:c.8826-274A>G MANE Select	ENSP00000261609.8:n.8826-274A>G
ENST00000650509.1:c.537-274A>G	ENSP00000496936.1:n.537-274A>G
ENST00000261609.11:c.8826-274A>G	ENSP00000261609.7:n.8826-274A>G
NM_004667.5:c.8826-274A>G	NP_004658.3:n.8826-274A>G
XM_005268276.3:c.8712-274A>G	XP_005268333.1:n.8712-274A>G
XM_005268277.3:c.8712-274A>G	XP_005268334.1:n.8712-274A>G
XM_006720726.2:c.8811-274A>G	XP_006720789.1:n.8811-274A>G
XM_006720727.2:c.8568-274A>G	XP_006720790.1:n.8568-274A>G
XM_011522131.1:c.8343-274A>G	XP_011520433.1:n.8343-274A>G
XM_011522132.1:c.6342-274A>G	XP_011520434.1:n.6342-274A>G
XM_011522133.1:c.5571-274A>G	XP_011520435.1:n.5571-274A>G
XM_011522134.1:c.2943-274A>G	XP_011520436.1:n.2943-274A>G
XR_931930.1:n.8955-274A>G
XM_005268276.5:c.8712-274A>G	XP_005268333.1:n.8712-274A>G
XM_006720726.3:c.8811-274A>G	XP_006720789.1:n.8811-274A>G
XM_006720727.3:c.8568-274A>G	XP_006720790.1:n.8568-274A>G
XM_017022695.1:c.8712-274A>G	XP_016878184.1:n.8712-274A>G
XM_017022696.1:c.8712-274A>G	XP_016878185.1:n.8712-274A>G
XM_017022697.1:c.1992-274A>G	XP_016878186.1:n.1992-274A>G
XM_017022698.1:c.1992-274A>G	XP_016878187.1:n.1992-274A>G
XR_931930.2:n.8956-274A>G
NM_004667.6:c.8826-274A>G MANE Select	NP_004658.3:n.8826-274A>G