Canonical Allele Identifier: CA434770738
Gene: CPOX HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.98304482T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585638T>G , CM000665.2:g.98585638T>G GRCh38
NC_000003.11:g.98304482T>G , CM000665.1:g.98304482T>G GRCh37
NC_000003.10:g.99787172T>G NCBI36
NG_015994.1:g.12974A>C
NG_015994.2:g.12974A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647941.2:c.975A>C MANE Select ENSP00000497326.1:p.Ile325=
ENST00000264193.2:c.975A>C ENSP00000264193.2:p.Ile325=
ENST00000510489.1:n.225A>C
NM_000097.5:c.975A>C NP_000088.3:p.Ile325=
XM_005247125.3:c.975A>C XP_005247182.1:p.Ile325=
NM_000097.7:c.975A>C MANE Select NP_000088.3:p.Ile325=
XM_005247125.4:c.975A>C XP_005247182.1:p.Ile325=
XR_001740025.2:n.1146A>C
XR_001740026.1:n.1710A>C
XR_001740027.1:n.1250A>C
XR_001740028.1:n.1216A>C