Canonical Allele Identifier: CA3289710
Gene: CD180 HGNC NCBI

Linked Data

dbSNP Id: rs774491929
ExAC: 5:66479912 T / C
gnomAD v2: 5-66479912-T-C
gnomAD v4: 5-67184084-T-C
MyVariant Identifiers: chr5:g.66479912T>C (hg19) chr5:g.67184084T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.67184084T>C , CM000667.2:g.67184084T>C GRCh38
NC_000005.9:g.66479912T>C , CM000667.1:g.66479912T>C GRCh37
NC_000005.8:g.66515668T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256447.5:c.759A>G MANE Select ENSP00000256447.4:p.Gly253=
NM_005582.2:c.759A>G NP_005573.2:p.Gly253=
XM_005248504.3:c.720A>G XP_005248561.1:p.Gly240=
XM_005248504.4:c.720A>G XP_005248561.1:p.Gly240=
NM_005582.3:c.759A>G MANE Select NP_005573.2:p.Gly253=
Search 100 bp 5'
Search 100 bp 3'