Canonical Allele Identifier: CA3289734
Gene: CD180 HGNC NCBI

Linked Data

ClinVar Variation Id: 757510
ClinVar RCV Id: RCV000935133
dbSNP Id: rs2230521
ExAC: 5:66480005 C / G
gnomAD v2: 5-66480005-C-G
gnomAD v3: 5-67184177-C-G
gnomAD v4: 5-67184177-C-G
MyVariant Identifiers: chr5:g.66480005C>G (hg19) chr5:g.67184177C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.67184177C>G , CM000667.2:g.67184177C>G GRCh38
NC_000005.9:g.66480005C>G , CM000667.1:g.66480005C>G GRCh37
NC_000005.8:g.66515761C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000256447.5:c.666G>C MANE Select ENSP00000256447.4:p.Thr222=
NM_005582.2:c.666G>C NP_005573.2:p.Thr222=
XM_005248504.3:c.627G>C XP_005248561.1:p.Thr209=
XM_005248504.4:c.627G>C XP_005248561.1:p.Thr209=
NM_005582.3:c.666G>C MANE Select NP_005573.2:p.Thr222=
Search 100 bp 5'
Search 100 bp 3'