Canonical Allele Identifier: CA31691460
Gene: FCGR2B HGNC NCBI

Linked Data

ClinVar Variation Id: 5466
ClinVar RCV Id: RCV000005799
dbSNP Id: rs3219018
gnomAD v3: 1-161662856-G-C
gnomAD v4: 1-161662856-G-C
MyVariant Identifiers: chr1:g.161632646G>C (hg19) chr1:g.161662856G>C (hg38)
PubMed: PMID:15895258
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161662856G>C , CM000663.2:g.161662856G>C GRCh38
NC_000001.10:g.161632646G>C , CM000663.1:g.161632646G>C GRCh37
NC_000001.9:g.159899270G>C NCBI36
NG_023318.1:g.4742G>C

Transcript Alleles

HGVS Amino-acid change
XM_017000670.2:c.-72-314G>C XP_016856159.1:n.-72-314G>C
XM_024454044.1:c.-72-314G>C XP_024309812.1:n.-72-314G>C
XM_024454045.1:c.-72-314G>C XP_024309813.1:n.-72-314G>C
XR_002959731.1:n.20-314G>C
NM_001002273.3:c.-72-314G>C NP_001002273.1:n.-72-314G>C
NM_001002274.3:c.-72-314G>C NP_001002274.1:n.-72-314G>C
NM_001002275.3:c.-72-314G>C NP_001002275.1:n.-72-314G>C
NM_001190828.2:c.-72-314G>C NP_001177757.1:n.-72-314G>C
NM_001386000.1:c.-72-314G>C NP_001372929.1:n.-72-314G>C
NM_001386001.1:c.-72-314G>C NP_001372930.1:n.-72-314G>C
NM_001386002.1:c.-72-314G>C NP_001372931.1:n.-72-314G>C
NM_001386003.1:c.-72-314G>C NP_001372932.1:n.-72-314G>C
NM_001386004.1:c.-72-314G>C NP_001372933.1:n.-72-314G>C
NM_001386005.1:c.-72-314G>C NP_001372934.1:n.-72-314G>C
NM_001386006.1:c.-72-314G>C NP_001372935.1:n.-72-314G>C
NM_004001.5:c.-72-314G>C NP_003992.3:n.-72-314G>C
NR_169827.1:n.20-314G>C
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