Canonical Allele Identifier: CA359908457
Gene: CD180 HGNC NCBI

Linked Data

gnomAD v4: 5-67184082-G-T
MyVariant Identifiers: chr5:g.66479910G>T (hg19) chr5:g.67184082G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.67184082G>T , CM000667.2:g.67184082G>T GRCh38
NC_000005.9:g.66479910G>T , CM000667.1:g.66479910G>T GRCh37
NC_000005.8:g.66515666G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256447.5:c.761C>A MANE Select ENSP00000256447.4:p.Thr254Lys
NM_005582.2:c.761C>A NP_005573.2:p.Thr254Lys
XM_005248504.3:c.722C>A XP_005248561.1:p.Thr241Lys
XM_005248504.4:c.722C>A XP_005248561.1:p.Thr241Lys
NM_005582.3:c.761C>A MANE Select NP_005573.2:p.Thr254Lys
Search 100 bp 5'
Search 100 bp 3'