Canonical Allele Identifier: CA353645008
Gene: CPOX HGNC NCBI

Linked Data

dbSNP Id: rs1239134864
gnomAD v2: 3-98304385-C-G
gnomAD v3: 3-98585541-C-G
gnomAD v4: 3-98585541-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585541C>G , CM000665.2:g.98585541C>G GRCh38
NC_000003.11:g.98304385C>G , CM000665.1:g.98304385C>G GRCh37
NC_000003.10:g.99787075C>G NCBI36
NG_015994.1:g.13071G>C
NG_015994.2:g.13071G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647941.2:c.1072G>C MANE Select ENSP00000497326.1:p.Ala358Pro
ENST00000264193.2:c.1072G>C ENSP00000264193.2:p.Ala358Pro
ENST00000510489.1:n.322G>C
NM_000097.5:c.1072G>C NP_000088.3:p.Ala358Pro
XM_005247125.3:c.1072G>C XP_005247182.1:p.Ala358Pro
NM_000097.7:c.1072G>C MANE Select NP_000088.3:p.Ala358Pro
XM_005247125.4:c.1072G>C XP_005247182.1:p.Ala358Pro
XR_001740025.2:n.1243G>C
XR_001740026.1:n.1807G>C
XR_001740027.1:n.1347G>C
XR_001740028.1:n.1313G>C