Canonical Allele Identifier: CA96644171
Gene: COMMD8 HGNC NCBI

Linked Data

dbSNP Id: rs375216374
MyVariant Identifiers: chr4:g.47462377C>T (hg19) chr4:g.47460360C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.47460360C>T , CM000666.2:g.47460360C>T GRCh38
NC_000004.11:g.47462377C>T , CM000666.1:g.47462377C>T GRCh37
NC_000004.10:g.47157134C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000381571.6:c.67-61G>A MANE Select ENSP00000370984.4:n.67-61G>A
ENST00000381571.5:c.67-61G>A ENSP00000370984.4:n.67-61G>A
ENST00000509220.1:n.81-61G>A
NM_017845.3:c.67-61G>A NP_060315.1:n.67-61G>A
XM_006714019.1:c.67-61G>A XP_006714082.1:n.67-61G>A
NM_001329668.1:c.67-61G>A NP_001316597.1:n.67-61G>A
NM_017845.4:c.67-61G>A NP_060315.1:n.67-61G>A
XM_017008330.1:c.67-61G>A XP_016863819.1:n.67-61G>A
NM_017845.5:c.67-61G>A MANE Select NP_060315.1:n.67-61G>A
NM_001329668.2:c.67-61G>A NP_001316597.1:n.67-61G>A
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