Canonical Allele Identifier: CA359908465
Gene: CD180 HGNC NCBI

Linked Data

gnomAD v4: 5-67184088-A-T
MyVariant Identifiers: chr5:g.66479916A>T (hg19) chr5:g.67184088A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.67184088A>T , CM000667.2:g.67184088A>T GRCh38
NC_000005.9:g.66479916A>T , CM000667.1:g.66479916A>T GRCh37
NC_000005.8:g.66515672A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256447.5:c.755T>A MANE Select ENSP00000256447.4:p.Leu252Gln
NM_005582.2:c.755T>A NP_005573.2:p.Leu252Gln
XM_005248504.3:c.716T>A XP_005248561.1:p.Leu239Gln
XM_005248504.4:c.716T>A XP_005248561.1:p.Leu239Gln
NM_005582.3:c.755T>A MANE Select NP_005573.2:p.Leu252Gln
Search 100 bp 5'
Search 100 bp 3'