Canonical Allele Identifier: CA1051334620

Gene: CPOX

Linked Data

• dbSNP Id: rs1707350069
• gnomAD v3: 3-98585741-G-C
• gnomAD v4: 3-98585741-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585741G>C , CM000665.2:g.98585741G>C	GRCh38
NC_000003.11:g.98304585G>C , CM000665.1:g.98304585G>C	GRCh37
NC_000003.10:g.99787275G>C	NCBI36
NG_015994.1:g.12871C>G
NG_015994.2:g.12871C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647941.2:c.954-82C>G MANE Select	ENSP00000497326.1:n.954-82C>G
ENST00000264193.2:c.954-82C>G	ENSP00000264193.2:n.954-82C>G
ENST00000510489.1:n.122C>G
NM_000097.5:c.954-82C>G	NP_000088.3:n.954-82C>G
XM_005247125.3:c.954-82C>G	XP_005247182.1:n.954-82C>G
NM_000097.7:c.954-82C>G MANE Select	NP_000088.3:n.954-82C>G
XM_005247125.4:c.954-82C>G	XP_005247182.1:n.954-82C>G
XR_001740025.2:n.1125-82C>G
XR_001740026.1:n.1607C>G
XR_001740027.1:n.1229-82C>G
XR_001740028.1:n.1195-82C>G