Canonical Allele Identifier: CA80083044
Gene: CPOX HGNC NCBI

Linked Data

dbSNP Id: rs771079616
gnomAD v4: 3-98585710-A-G
MyVariant Identifiers: chr3:g.98304554A>G (hg19) chr3:g.98585710A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585710A>G , CM000665.2:g.98585710A>G GRCh38
NC_000003.11:g.98304554A>G , CM000665.1:g.98304554A>G GRCh37
NC_000003.10:g.99787244A>G NCBI36
NG_015994.1:g.12902T>C
NG_015994.2:g.12902T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.954-51T>C MANE Select ENSP00000497326.1:n.954-51T>C
ENST00000264193.2:c.954-51T>C ENSP00000264193.2:n.954-51T>C
ENST00000510489.1:n.153T>C
NM_000097.5:c.954-51T>C NP_000088.3:n.954-51T>C
XM_005247125.3:c.954-51T>C XP_005247182.1:n.954-51T>C
NM_000097.7:c.954-51T>C MANE Select NP_000088.3:n.954-51T>C
XM_005247125.4:c.954-51T>C XP_005247182.1:n.954-51T>C
XR_001740025.2:n.1125-51T>C
XR_001740026.1:n.1638T>C
XR_001740027.1:n.1229-51T>C
XR_001740028.1:n.1195-51T>C
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