Canonical Allele Identifier: CA561955006
Gene: COMMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.116392141G>A , CM000667.2:g.116392141G>A GRCh38
NC_000005.9:g.115727838G>A , CM000667.1:g.115727838G>A GRCh37
NC_000005.8:g.115755737G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000503424.1:n.582-7341G>A
XR_948268.1:n.1205-7341G>A
XR_948269.1:n.1209-7341G>A
XR_948270.1:n.1034-7341G>A
XM_017009557.1:c.177-7341G>A XP_016865046.1:n.177-7341G>A
XR_001742095.2:n.6342-7341G>A
XR_001742096.2:n.6346-7341G>A
XR_001742099.2:n.6261-7341G>A
XR_002956162.1:n.1034-54023G>A
XR_948270.2:n.1034-7341G>A