Canonical Allele Identifier: CA1455346827

Gene: COMMD8

Linked Data

• dbSNP Id: rs1729994455

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.47460356T>C , CM000666.2:g.47460356T>C	GRCh38
NC_000004.11:g.47462373T>C , CM000666.1:g.47462373T>C	GRCh37
NC_000004.10:g.47157130T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381571.6:c.67-57A>G MANE Select	ENSP00000370984.4:n.67-57A>G
ENST00000381571.5:c.67-57A>G	ENSP00000370984.4:n.67-57A>G
ENST00000509220.1:n.81-57A>G
NM_017845.3:c.67-57A>G	NP_060315.1:n.67-57A>G
XM_006714019.1:c.67-57A>G	XP_006714082.1:n.67-57A>G
NM_001329668.1:c.67-57A>G	NP_001316597.1:n.67-57A>G
NM_017845.4:c.67-57A>G	NP_060315.1:n.67-57A>G
XM_017008330.1:c.67-57A>G	XP_016863819.1:n.67-57A>G
NM_017845.5:c.67-57A>G MANE Select	NP_060315.1:n.67-57A>G
NM_001329668.2:c.67-57A>G	NP_001316597.1:n.67-57A>G