Canonical Allele Identifier: CA2670531472
Gene: COMMD8 HGNC NCBI

Linked Data

gnomAD v4: 4-47460418-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.47460418A>T , CM000666.2:g.47460418A>T GRCh38
NC_000004.11:g.47462435A>T , CM000666.1:g.47462435A>T GRCh37
NC_000004.10:g.47157192A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000381571.6:c.67-119T>A MANE Select ENSP00000370984.4:n.67-119T>A
ENST00000381571.5:c.67-119T>A ENSP00000370984.4:n.67-119T>A
ENST00000509220.1:n.81-119T>A
NM_017845.3:c.67-119T>A NP_060315.1:n.67-119T>A
XM_006714019.1:c.67-119T>A XP_006714082.1:n.67-119T>A
NM_001329668.1:c.67-119T>A NP_001316597.1:n.67-119T>A
NM_017845.4:c.67-119T>A NP_060315.1:n.67-119T>A
XM_017008330.1:c.67-119T>A XP_016863819.1:n.67-119T>A
NM_017845.5:c.67-119T>A MANE Select NP_060315.1:n.67-119T>A
NM_001329668.2:c.67-119T>A NP_001316597.1:n.67-119T>A
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