Canonical Allele Identifier: CA2666706690
Gene: CPOX HGNC NCBI

Linked Data

gnomAD v4: 3-98585727-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585727C>T , CM000665.2:g.98585727C>T GRCh38
NC_000003.11:g.98304571C>T , CM000665.1:g.98304571C>T GRCh37
NC_000003.10:g.99787261C>T NCBI36
NG_015994.1:g.12885G>A
NG_015994.2:g.12885G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.954-68G>A MANE Select ENSP00000497326.1:n.954-68G>A
ENST00000264193.2:c.954-68G>A ENSP00000264193.2:n.954-68G>A
ENST00000510489.1:n.136G>A
NM_000097.5:c.954-68G>A NP_000088.3:n.954-68G>A
XM_005247125.3:c.954-68G>A XP_005247182.1:n.954-68G>A
NM_000097.7:c.954-68G>A MANE Select NP_000088.3:n.954-68G>A
XM_005247125.4:c.954-68G>A XP_005247182.1:n.954-68G>A
XR_001740025.2:n.1125-68G>A
XR_001740026.1:n.1621G>A
XR_001740027.1:n.1229-68G>A
XR_001740028.1:n.1195-68G>A
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