Canonical Allele Identifier: CA359908684
Gene: CD180 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.66480013C>A (hg19) chr5:g.67184185C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.67184185C>A , CM000667.2:g.67184185C>A GRCh38
NC_000005.9:g.66480013C>A , CM000667.1:g.66480013C>A GRCh37
NC_000005.8:g.66515769C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000256447.5:c.658G>T MANE Select ENSP00000256447.4:p.Asp220Tyr
NM_005582.2:c.658G>T NP_005573.2:p.Asp220Tyr
XM_005248504.3:c.619G>T XP_005248561.1:p.Asp207Tyr
XM_005248504.4:c.619G>T XP_005248561.1:p.Asp207Tyr
NM_005582.3:c.658G>T MANE Select NP_005573.2:p.Asp220Tyr
Search 100 bp 5'
Search 100 bp 3'