Canonical Allele Identifier: CA3289711
Gene: CD180 HGNC NCBI

Linked Data

dbSNP Id: rs748438480
ExAC: 5:66479913 C / T
gnomAD v2: 5-66479913-C-T
gnomAD v3: 5-67184085-C-T
gnomAD v4: 5-67184085-C-T
COSMIC: COSM3920287
MyVariant Identifiers: chr5:g.66479913C>T (hg19) chr5:g.67184085C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.67184085C>T , CM000667.2:g.67184085C>T GRCh38
NC_000005.9:g.66479913C>T , CM000667.1:g.66479913C>T GRCh37
NC_000005.8:g.66515669C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256447.5:c.758G>A MANE Select ENSP00000256447.4:p.Gly253Glu
NM_005582.2:c.758G>A NP_005573.2:p.Gly253Glu
XM_005248504.3:c.719G>A XP_005248561.1:p.Gly240Glu
XM_005248504.4:c.719G>A XP_005248561.1:p.Gly240Glu
NM_005582.3:c.758G>A MANE Select NP_005573.2:p.Gly253Glu
Search 100 bp 5'
Search 100 bp 3'