Canonical Allele Identifier: CA353644943
Gene: CPOX HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.98304354A>C (hg19) chr3:g.98585510A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585510A>C , CM000665.2:g.98585510A>C GRCh38
NC_000003.11:g.98304354A>C , CM000665.1:g.98304354A>C GRCh37
NC_000003.10:g.99787044A>C NCBI36
NG_015994.1:g.13102T>G
NG_015994.2:g.13102T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.1103T>G MANE Select ENSP00000497326.1:p.Leu368Arg
ENST00000264193.2:c.1103T>G ENSP00000264193.2:p.Leu368Arg
ENST00000510489.1:n.353T>G
NM_000097.5:c.1103T>G NP_000088.3:p.Leu368Arg
XM_005247125.3:c.1103T>G XP_005247182.1:p.Leu368Arg
NM_000097.7:c.1103T>G MANE Select NP_000088.3:p.Leu368Arg
XM_005247125.4:c.1103T>G XP_005247182.1:p.Leu368Arg
XR_001740025.2:n.1274T>G
XR_001740026.1:n.1838T>G
XR_001740027.1:n.1378T>G
XR_001740028.1:n.1344T>G
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