Canonical Allele Identifier: CA434770617
Gene: CPOX HGNC NCBI

Linked Data

dbSNP Id: rs1314263561
gnomAD v4: 3-98585485-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585485T>G , CM000665.2:g.98585485T>G GRCh38
NC_000003.11:g.98304329T>G , CM000665.1:g.98304329T>G GRCh37
NC_000003.10:g.99787019T>G NCBI36
NG_015994.1:g.13127A>C
NG_015994.2:g.13127A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000512905.6:c.14A>C
ENST00000647941.2:c.1128A>C MANE Select ENSP00000497326.1:p.Ser376=
ENST00000264193.2:c.1128A>C ENSP00000264193.2:p.Ser376=
ENST00000510489.1:n.378A>C
ENST00000512905.5:c.14A>C
NM_000097.5:c.1128A>C NP_000088.3:p.Ser376=
XM_005247125.3:c.1128A>C XP_005247182.1:p.Ser376=
NM_000097.7:c.1128A>C MANE Select NP_000088.3:p.Ser376=
XM_005247125.4:c.1128A>C XP_005247182.1:p.Ser376=
XR_001740025.2:n.1299A>C
XR_001740026.1:n.1863A>C
XR_001740027.1:n.1403A>C
XR_001740028.1:n.1369A>C