Canonical Allele Identifier: CA444672481
Gene: CD180 HGNC NCBI

Linked Data

gnomAD v4: 5-67184189-A-C
MyVariant Identifiers: chr5:g.66480017A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.67184189A>C , CM000667.2:g.67184189A>C GRCh38
NC_000005.9:g.66480017A>C , CM000667.1:g.66480017A>C GRCh37
NC_000005.8:g.66515773A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256447.5:c.654T>G MANE Select ENSP00000256447.4:p.Ala218=
NM_005582.2:c.654T>G NP_005573.2:p.Ala218=
XM_005248504.3:c.615T>G XP_005248561.1:p.Ala205=
XM_005248504.4:c.615T>G XP_005248561.1:p.Ala205=
NM_005582.3:c.654T>G MANE Select NP_005573.2:p.Ala218=
Search 100 bp 5'
Search 100 bp 3'