Canonical Allele Identifier: CA353645207
Gene: CPOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585634G>T , CM000665.2:g.98585634G>T GRCh38
NC_000003.11:g.98304478G>T , CM000665.1:g.98304478G>T GRCh37
NC_000003.10:g.99787168G>T NCBI36
NG_015994.1:g.12978C>A
NG_015994.2:g.12978C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647941.2:c.979C>A MANE Select ENSP00000497326.1:p.His327Asn
ENST00000264193.2:c.979C>A ENSP00000264193.2:p.His327Asn
ENST00000510489.1:n.229C>A
NM_000097.5:c.979C>A NP_000088.3:p.His327Asn
XM_005247125.3:c.979C>A XP_005247182.1:p.His327Asn
NM_000097.7:c.979C>A MANE Select NP_000088.3:p.His327Asn
XM_005247125.4:c.979C>A XP_005247182.1:p.His327Asn
XR_001740025.2:n.1150C>A
XR_001740026.1:n.1714C>A
XR_001740027.1:n.1254C>A
XR_001740028.1:n.1220C>A