Canonical Allele Identifier: CA359908454
Gene: CD180 HGNC NCBI

Linked Data

dbSNP Id: rs1409966388
gnomAD v3: 5-67184080-A-G
gnomAD v4: 5-67184080-A-G
MyVariant Identifiers: chr5:g.66479908A>G (hg19) chr5:g.67184080A>G (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000256447.5:c.763T>C MANE Select ENSP00000256447.4:p.Phe255Leu
NM_005582.2:c.763T>C NP_005573.2:p.Phe255Leu
XM_005248504.3:c.724T>C XP_005248561.1:p.Phe242Leu
XM_005248504.4:c.724T>C XP_005248561.1:p.Phe242Leu
NM_005582.3:c.763T>C MANE Select NP_005573.2:p.Phe255Leu
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