Canonical Allele Identifier: CA917495393
Gene: CD180 HGNC NCBI

Linked Data

dbSNP Id: rs1554036028
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.67184176del , CM000667.2:g.67184176del GRCh38
NC_000005.9:g.66480004del , CM000667.1:g.66480004del GRCh37
NC_000005.8:g.66515760del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256447.5:c.667del MANE Select ENSP00000256447.4:p.Ile223SerfsTer5
NM_005582.2:c.667del NP_005573.2:p.Ile223SerfsTer5
XM_005248504.3:c.628del XP_005248561.1:p.Ile210SerfsTer5
XM_005248504.4:c.628del XP_005248561.1:p.Ile210SerfsTer5
NM_005582.3:c.667del MANE Select NP_005573.2:p.Ile223SerfsTer5
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