Canonical Allele Identifier: CA434770719

Gene: CPOX

Linked Data

• MyVariant Identifiers: chr3:g.98304464C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585620C>A , CM000665.2:g.98585620C>A	GRCh38
NC_000003.11:g.98304464C>A , CM000665.1:g.98304464C>A	GRCh37
NC_000003.10:g.99787154C>A	NCBI36
NG_015994.1:g.12992G>T
NG_015994.2:g.12992G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647941.2:c.993G>T MANE Select	ENSP00000497326.1:p.Arg331=
ENST00000264193.2:c.993G>T	ENSP00000264193.2:p.Arg331=
ENST00000510489.1:n.243G>T
NM_000097.5:c.993G>T	NP_000088.3:p.Arg331=
XM_005247125.3:c.993G>T	XP_005247182.1:p.Arg331=
NM_000097.7:c.993G>T MANE Select	NP_000088.3:p.Arg331=
XM_005247125.4:c.993G>T	XP_005247182.1:p.Arg331=
XR_001740025.2:n.1164G>T
XR_001740026.1:n.1728G>T
XR_001740027.1:n.1268G>T
XR_001740028.1:n.1234G>T