Canonical Allele Identifier: CA359908674
Gene: CD180 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.66480010A>T (hg19) chr5:g.67184182A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.67184182A>T , CM000667.2:g.67184182A>T GRCh38
NC_000005.9:g.66480010A>T , CM000667.1:g.66480010A>T GRCh37
NC_000005.8:g.66515766A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000256447.5:c.661T>A MANE Select ENSP00000256447.4:p.Ser221Thr
NM_005582.2:c.661T>A NP_005573.2:p.Ser221Thr
XM_005248504.3:c.622T>A XP_005248561.1:p.Ser208Thr
XM_005248504.4:c.622T>A XP_005248561.1:p.Ser208Thr
NM_005582.3:c.661T>A MANE Select NP_005573.2:p.Ser221Thr
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