Canonical Allele Identifier: CA444672479
Gene: CD180 HGNC NCBI

Linked Data

gnomAD v4: 5-67184186-A-G
MyVariant Identifiers: chr5:g.66480014A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.67184186A>G , CM000667.2:g.67184186A>G GRCh38
NC_000005.9:g.66480014A>G , CM000667.1:g.66480014A>G GRCh37
NC_000005.8:g.66515770A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256447.5:c.657T>C MANE Select ENSP00000256447.4:p.Phe219=
NM_005582.2:c.657T>C NP_005573.2:p.Phe219=
XM_005248504.3:c.618T>C XP_005248561.1:p.Phe206=
XM_005248504.4:c.618T>C XP_005248561.1:p.Phe206=
NM_005582.3:c.657T>C MANE Select NP_005573.2:p.Phe219=
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