Canonical Allele Identifier: CA359908664
Gene: CD180 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.66480007T>G (hg19) chr5:g.67184179T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.67184179T>G , CM000667.2:g.67184179T>G GRCh38
NC_000005.9:g.66480007T>G , CM000667.1:g.66480007T>G GRCh37
NC_000005.8:g.66515763T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000256447.5:c.664A>C MANE Select ENSP00000256447.4:p.Thr222Pro
NM_005582.2:c.664A>C NP_005573.2:p.Thr222Pro
XM_005248504.3:c.625A>C XP_005248561.1:p.Thr209Pro
XM_005248504.4:c.625A>C XP_005248561.1:p.Thr209Pro
NM_005582.3:c.664A>C MANE Select NP_005573.2:p.Thr222Pro
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