Canonical Allele Identifier: CA916961979
Gene: CPOX HGNC NCBI

Linked Data

dbSNP Id: rs1559676168

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585641_98585661dup , CM000665.2:g.98585641_98585661dup GRCh38
NC_000003.11:g.98304485_98304505dup , CM000665.1:g.98304485_98304505dup GRCh37
NC_000003.10:g.99787175_99787195dup NCBI36
NG_015994.1:g.12952_12972dup
NG_015994.2:g.12952_12972dup

Transcript Alleles

HGVS Amino-acid change
ENST00000647941.2:c.954-1_973dup
ENST00000264193.2:c.954-1_973dup
ENST00000510489.1:n.203_223dup
NM_000097.5:c.954-1_973dup
XM_005247125.3:c.954-1_973dup
NM_000097.7:c.954-1_973dup
XM_005247125.4:c.954-1_973dup
XR_001740025.2:n.1125-1_1144dup
XR_001740026.1:n.1688_1708dup
XR_001740027.1:n.1229-1_1248dup
XR_001740028.1:n.1195-1_1214dup