Canonical Allele Identifier: CA1552876078
Gene: CD180 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.67184080A= , CM000667.2:g.67184080A= GRCh38
NC_000005.9:g.66479908A= , CM000667.1:g.66479908A= GRCh37
NC_000005.8:g.66515664A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256447.5:c.763T= MANE Select ENSP00000256447.4:p.Phe255=
NM_005582.2:c.763T= NP_005573.2:p.Phe255=
XM_005248504.3:c.724T= XP_005248561.1:p.Phe242=
XM_005248504.4:c.724T= XP_005248561.1:p.Phe242=
NM_005582.3:c.763T= MANE Select NP_005573.2:p.Phe255=
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