Canonical Allele Identifier: CA135105523
Gene: CD83 HGNC NCBI

Linked Data

dbSNP Id: rs1021794515
gnomAD v3: 6-14133957-G-C
gnomAD v4: 6-14133957-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.14133957G>C , CM000668.2:g.14133957G>C GRCh38
NC_000006.11:g.14134188G>C , CM000668.1:g.14134188G>C GRCh37
NC_000006.10:g.14242167G>C NCBI36
NG_030372.1:g.21702G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000379153.4:c.489+202G>C MANE Select ENSP00000368450.3:n.489+202G>C
ENST00000379153.3:c.489+202G>C ENSP00000368450.3:n.489+202G>C
ENST00000612003.4:c.312+202G>C ENSP00000480760.1:n.312+202G>C
NM_001040280.1:c.489+202G>C NP_001035370.1:n.489+202G>C
NM_001251901.1:c.312+202G>C NP_001238830.1:n.312+202G>C
NM_004233.3:c.489+202G>C NP_004224.1:n.489+202G>C
NM_004233.4:c.489+202G>C MANE Select NP_004224.1:n.489+202G>C
NM_001040280.2:c.489+202G>C NP_001035370.1:n.489+202G>C
NM_001040280.3:c.489+202G>C NP_001035370.1:n.489+202G>C