Canonical Allele Identifier: CA434770720

Gene: CPOX

Linked Data

• gnomAD v4: 3-98585622-G-T
• MyVariant Identifiers: chr3:g.98304466G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585622G>T , CM000665.2:g.98585622G>T	GRCh38
NC_000003.11:g.98304466G>T , CM000665.1:g.98304466G>T	GRCh37
NC_000003.10:g.99787156G>T	NCBI36
NG_015994.1:g.12990C>A
NG_015994.2:g.12990C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647941.2:c.991C>A MANE Select	ENSP00000497326.1:p.Arg331=
ENST00000264193.2:c.991C>A	ENSP00000264193.2:p.Arg331=
ENST00000510489.1:n.241C>A
NM_000097.5:c.991C>A	NP_000088.3:p.Arg331=
XM_005247125.3:c.991C>A	XP_005247182.1:p.Arg331=
NM_000097.7:c.991C>A MANE Select	NP_000088.3:p.Arg331=
XM_005247125.4:c.991C>A	XP_005247182.1:p.Arg331=
XR_001740025.2:n.1162C>A
XR_001740026.1:n.1726C>A
XR_001740027.1:n.1266C>A
XR_001740028.1:n.1232C>A