Canonical Allele Identifier: CA7439634

Gene: HERC2

Linked Data

• dbSNP Id: rs760015880
• ExAC: 15:28356867 T / C
• gnomAD v2: 15-28356867-T-C
• gnomAD v3: 15-28111721-T-C
• gnomAD v4: 15-28111721-T-C
• MyVariant Identifiers: chr15:g.28356867T>C (hg19) ; chr15:g.28111721T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28111721T>C , CM000677.2:g.28111721T>C	GRCh38
NC_000015.9:g.28356867T>C , CM000677.1:g.28356867T>C	GRCh37
NC_000015.8:g.26030462T>C	NCBI36
NG_016355.1:g.215429A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261609.13:c.*42A>G MANE Select	ENSP00000261609.8:n.*42A>G
ENST00000650509.1:c.6026A>G	ENSP00000496936.1:n.6026A>G
ENST00000261609.11:c.*42A>G	ENSP00000261609.7:n.*42A>G
ENST00000566635.5:n.1672A>G
NM_004667.5:c.*42A>G	NP_004658.3:n.*42A>G
XM_005268276.3:c.*42A>G	XP_005268333.1:n.*42A>G
XM_005268277.3:c.*42A>G	XP_005268334.1:n.*42A>G
XM_006720726.2:c.*42A>G	XP_006720789.1:n.*42A>G
XM_006720727.2:c.*42A>G	XP_006720790.1:n.*42A>G
XM_011522131.1:c.*42A>G	XP_011520433.1:n.*42A>G
XM_011522132.1:c.*42A>G	XP_011520434.1:n.*42A>G
XM_011522133.1:c.*42A>G	XP_011520435.1:n.*42A>G
XM_011522134.1:c.*42A>G	XP_011520436.1:n.*42A>G
XM_005268276.5:c.*42A>G	XP_005268333.1:n.*42A>G
XM_006720726.3:c.*42A>G	XP_006720789.1:n.*42A>G
XM_006720727.3:c.*42A>G	XP_006720790.1:n.*42A>G
XM_017022695.1:c.*42A>G	XP_016878184.1:n.*42A>G
XM_017022696.1:c.*42A>G	XP_016878185.1:n.*42A>G
XM_017022697.1:c.*42A>G	XP_016878186.1:n.*42A>G
XM_017022698.1:c.*42A>G	XP_016878187.1:n.*42A>G
NM_004667.6:c.*42A>G MANE Select	NP_004658.3:n.*42A>G