Canonical Allele Identifier: CA359908671
Gene: CD180 HGNC NCBI

Linked Data

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

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000256447.5:c.661T>G MANE Select ENSP00000256447.4:p.Ser221Ala
NM_005582.2:c.661T>G NP_005573.2:p.Ser221Ala
XM_005248504.3:c.622T>G XP_005248561.1:p.Ser208Ala
XM_005248504.4:c.622T>G XP_005248561.1:p.Ser208Ala
NM_005582.3:c.661T>G MANE Select NP_005573.2:p.Ser221Ala
Search 100 bp 5'
Search 100 bp 3'