Canonical Allele Identifier: CA784180015

Gene: CPOX

Linked Data

• dbSNP Id: rs1310037290
• gnomAD v3: 3-98585764-G-C
• gnomAD v4: 3-98585764-G-C
• MyVariant Identifiers: chr3:g.98304608G>C (hg19) ; chr3:g.98585764G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585764G>C , CM000665.2:g.98585764G>C	GRCh38
NC_000003.11:g.98304608G>C , CM000665.1:g.98304608G>C	GRCh37
NC_000003.10:g.99787298G>C	NCBI36
NG_015994.1:g.12848C>G
NG_015994.2:g.12848C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647941.2:c.954-105C>G MANE Select	ENSP00000497326.1:n.954-105C>G
ENST00000264193.2:c.954-105C>G	ENSP00000264193.2:n.954-105C>G
ENST00000510489.1:n.99C>G
NM_000097.5:c.954-105C>G	NP_000088.3:n.954-105C>G
XM_005247125.3:c.954-105C>G	XP_005247182.1:n.954-105C>G
NM_000097.7:c.954-105C>G MANE Select	NP_000088.3:n.954-105C>G
XM_005247125.4:c.954-105C>G	XP_005247182.1:n.954-105C>G
XR_001740025.2:n.1125-105C>G
XR_001740026.1:n.1584C>G
XR_001740027.1:n.1229-105C>G
XR_001740028.1:n.1195-105C>G