Canonical Allele Identifier: CA359908662
Gene: CD180 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.66480006G>C (hg19) chr5:g.67184178G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.67184178G>C , CM000667.2:g.67184178G>C GRCh38
NC_000005.9:g.66480006G>C , CM000667.1:g.66480006G>C GRCh37
NC_000005.8:g.66515762G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000256447.5:c.665C>G MANE Select ENSP00000256447.4:p.Thr222Arg
NM_005582.2:c.665C>G NP_005573.2:p.Thr222Arg
XM_005248504.3:c.626C>G XP_005248561.1:p.Thr209Arg
XM_005248504.4:c.626C>G XP_005248561.1:p.Thr209Arg
NM_005582.3:c.665C>G MANE Select NP_005573.2:p.Thr222Arg
Search 100 bp 5'
Search 100 bp 3'