Canonical Allele Identifier: CA359908663
Gene: CD180 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.66480006G>T (hg19) chr5:g.67184178G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.67184178G>T , CM000667.2:g.67184178G>T GRCh38
NC_000005.9:g.66480006G>T , CM000667.1:g.66480006G>T GRCh37
NC_000005.8:g.66515762G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000256447.5:c.665C>A MANE Select ENSP00000256447.4:p.Thr222Lys
NM_005582.2:c.665C>A NP_005573.2:p.Thr222Lys
XM_005248504.3:c.626C>A XP_005248561.1:p.Thr209Lys
XM_005248504.4:c.626C>A XP_005248561.1:p.Thr209Lys
NM_005582.3:c.665C>A MANE Select NP_005573.2:p.Thr222Lys
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