Canonical Allele Identifier: CA2666706676
Gene: CPOX HGNC NCBI

Linked Data

gnomAD v4: 3-98585705-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585705C>T , CM000665.2:g.98585705C>T GRCh38
NC_000003.11:g.98304549C>T , CM000665.1:g.98304549C>T GRCh37
NC_000003.10:g.99787239C>T NCBI36
NG_015994.1:g.12907G>A
NG_015994.2:g.12907G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.954-46G>A MANE Select ENSP00000497326.1:n.954-46G>A
ENST00000264193.2:c.954-46G>A ENSP00000264193.2:n.954-46G>A
ENST00000510489.1:n.158G>A
NM_000097.5:c.954-46G>A NP_000088.3:n.954-46G>A
XM_005247125.3:c.954-46G>A XP_005247182.1:n.954-46G>A
NM_000097.7:c.954-46G>A MANE Select NP_000088.3:n.954-46G>A
XM_005247125.4:c.954-46G>A XP_005247182.1:n.954-46G>A
XR_001740025.2:n.1125-46G>A
XR_001740026.1:n.1643G>A
XR_001740027.1:n.1229-46G>A
XR_001740028.1:n.1195-46G>A