Canonical Allele Identifier: CA353645186

Gene: CPOX

Linked Data

• dbSNP Id: rs1729995
• MyVariant Identifiers: chr3:g.98304467T>G (hg19) ; chr3:g.98585623T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585623T>G , CM000665.2:g.98585623T>G	GRCh38
NC_000003.11:g.98304467T>G , CM000665.1:g.98304467T>G	GRCh37
NC_000003.10:g.99787157T>G	NCBI36
NG_015994.1:g.12989A>C
NG_015994.2:g.12989A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647941.2:c.990A>C MANE Select	ENSP00000497326.1:p.Glu330Asp
ENST00000264193.2:c.990A>C	ENSP00000264193.2:p.Glu330Asp
ENST00000510489.1:n.240A>C
NM_000097.5:c.990A>C	NP_000088.3:p.Glu330Asp
XM_005247125.3:c.990A>C	XP_005247182.1:p.Glu330Asp
NM_000097.7:c.990A>C MANE Select	NP_000088.3:p.Glu330Asp
XM_005247125.4:c.990A>C	XP_005247182.1:p.Glu330Asp
XR_001740025.2:n.1161A>C
XR_001740026.1:n.1725A>C
XR_001740027.1:n.1265A>C
XR_001740028.1:n.1231A>C