Canonical Allele Identifier: CA353644999
Gene: CPOX HGNC NCBI

Linked Data

dbSNP Id: rs1707345051
gnomAD v3: 3-98585536-C-A
gnomAD v4: 3-98585536-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585536C>A , CM000665.2:g.98585536C>A GRCh38
NC_000003.11:g.98304380C>A , CM000665.1:g.98304380C>A GRCh37
NC_000003.10:g.99787070C>A NCBI36
NG_015994.1:g.13076G>T
NG_015994.2:g.13076G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647941.2:c.1077G>T MANE Select ENSP00000497326.1:p.Arg359Ser
ENST00000264193.2:c.1077G>T ENSP00000264193.2:p.Arg359Ser
ENST00000510489.1:n.327G>T
NM_000097.5:c.1077G>T NP_000088.3:p.Arg359Ser
XM_005247125.3:c.1077G>T XP_005247182.1:p.Arg359Ser
NM_000097.7:c.1077G>T MANE Select NP_000088.3:p.Arg359Ser
XM_005247125.4:c.1077G>T XP_005247182.1:p.Arg359Ser
XR_001740025.2:n.1248G>T
XR_001740026.1:n.1812G>T
XR_001740027.1:n.1352G>T
XR_001740028.1:n.1318G>T