Canonical Allele Identifier: CA353644779

Gene: CPOX

Linked Data

• dbSNP Id: rs1175622037
• MyVariant Identifiers: chr3:g.98304283A>C (hg19) ; chr3:g.98585439A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585439A>C , CM000665.2:g.98585439A>C	GRCh38
NC_000003.11:g.98304283A>C , CM000665.1:g.98304283A>C	GRCh37
NC_000003.10:g.99786973A>C	NCBI36
NG_015994.1:g.13173T>G
NG_015994.2:g.13173T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000512905.6:c.58+2T>G
ENST00000647941.2:c.1172+2T>G MANE Select	ENSP00000497326.1:n.1172+2T>G
ENST00000264193.2:c.1172+2T>G	ENSP00000264193.2:n.1172+2T>G
ENST00000510489.1:n.422+2T>G
ENST00000512905.5:c.58+2T>G
NM_000097.5:c.1172+2T>G	NP_000088.3:n.1172+2T>G
XM_005247125.3:c.1172+2T>G	XP_005247182.1:n.1172+2T>G
NM_000097.7:c.1172+2T>G MANE Select	NP_000088.3:n.1172+2T>G
XM_005247125.4:c.1172+2T>G	XP_005247182.1:n.1172+2T>G
XR_001740025.2:n.1343+2T>G
XR_001740026.1:n.1907+2T>G
XR_001740027.1:n.1447+2T>G
XR_001740028.1:n.1413+2T>G