Canonical Allele Identifier: CA359908667
Gene: CD180 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.66480009G>A (hg19) chr5:g.67184181G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.67184181G>A , CM000667.2:g.67184181G>A GRCh38
NC_000005.9:g.66480009G>A , CM000667.1:g.66480009G>A GRCh37
NC_000005.8:g.66515765G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256447.5:c.662C>T MANE Select ENSP00000256447.4:p.Ser221Leu
NM_005582.2:c.662C>T NP_005573.2:p.Ser221Leu
XM_005248504.3:c.623C>T XP_005248561.1:p.Ser208Leu
XM_005248504.4:c.623C>T XP_005248561.1:p.Ser208Leu
NM_005582.3:c.662C>T MANE Select NP_005573.2:p.Ser221Leu
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