Canonical Allele Identifier: CA11941140

Gene: COMMD10

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.116423793G>A , CM000667.2:g.116423793G>A	GRCh38
NC_000005.9:g.115759490G>A , CM000667.1:g.115759490G>A	GRCh37
NC_000005.8:g.115787389G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_017009557.1:c.318-22371G>A	XP_016865046.1:n.318-22371G>A
XR_001742095.2:n.6483-22371G>A
XR_001742096.2:n.6487-22371G>A
XR_001742099.2:n.6402-22371G>A
XR_002956162.1:n.1034-22371G>A