Canonical Allele Identifier: CA3289712
Gene: CD180 HGNC NCBI

Linked Data

dbSNP Id: rs770702811
ExAC: 5:66479914 C / T
gnomAD v2: 5-66479914-C-T
gnomAD v4: 5-67184086-C-T
MyVariant Identifiers: chr5:g.66479914C>T (hg19) chr5:g.67184086C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.67184086C>T , CM000667.2:g.67184086C>T GRCh38
NC_000005.9:g.66479914C>T , CM000667.1:g.66479914C>T GRCh37
NC_000005.8:g.66515670C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256447.5:c.757G>A MANE Select ENSP00000256447.4:p.Gly253Arg
NM_005582.2:c.757G>A NP_005573.2:p.Gly253Arg
XM_005248504.3:c.718G>A XP_005248561.1:p.Gly240Arg
XM_005248504.4:c.718G>A XP_005248561.1:p.Gly240Arg
NM_005582.3:c.757G>A MANE Select NP_005573.2:p.Gly253Arg
Search 100 bp 5'
Search 100 bp 3'