Canonical Allele Identifier: CA434770723

Gene: CPOX

Linked Data

• MyVariant Identifiers: chr3:g.98304470T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585626T>G , CM000665.2:g.98585626T>G	GRCh38
NC_000003.11:g.98304470T>G , CM000665.1:g.98304470T>G	GRCh37
NC_000003.10:g.99787160T>G	NCBI36
NG_015994.1:g.12986A>C
NG_015994.2:g.12986A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647941.2:c.987A>C MANE Select	ENSP00000497326.1:p.Gly329=
ENST00000264193.2:c.987A>C	ENSP00000264193.2:p.Gly329=
ENST00000510489.1:n.237A>C
NM_000097.5:c.987A>C	NP_000088.3:p.Gly329=
XM_005247125.3:c.987A>C	XP_005247182.1:p.Gly329=
NM_000097.7:c.987A>C MANE Select	NP_000088.3:p.Gly329=
XM_005247125.4:c.987A>C	XP_005247182.1:p.Gly329=
XR_001740025.2:n.1158A>C
XR_001740026.1:n.1722A>C
XR_001740027.1:n.1262A>C
XR_001740028.1:n.1228A>C