Canonical Allele Identifier: CA2511515
Gene: CPOX HGNC NCBI

Linked Data

dbSNP Id: rs201231166
gnomAD v2: 3-98304319-G-A
gnomAD v4: 3-98585475-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585475G>A , CM000665.2:g.98585475G>A GRCh38
NC_000003.11:g.98304319G>A , CM000665.1:g.98304319G>A GRCh37
NC_000003.10:g.99787009G>A NCBI36
NG_015994.1:g.13137C>T
NG_015994.2:g.13137C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000512905.6:c.24C>T
ENST00000647941.2:c.1138C>T MANE Select ENSP00000497326.1:p.Gln380Ter
ENST00000264193.2:c.1138C>T ENSP00000264193.2:p.Gln380Ter
ENST00000510489.1:n.388C>T
ENST00000512905.5:c.24C>T
NM_000097.5:c.1138C>T NP_000088.3:p.Gln380Ter
XM_005247125.3:c.1138C>T XP_005247182.1:p.Gln380Ter
NM_000097.7:c.1138C>T MANE Select NP_000088.3:p.Gln380Ter
XM_005247125.4:c.1138C>T XP_005247182.1:p.Gln380Ter
XR_001740025.2:n.1309C>T
XR_001740026.1:n.1873C>T
XR_001740027.1:n.1413C>T
XR_001740028.1:n.1379C>T