Canonical Allele Identifier: CA1611669855
Gene: CD83 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.14133900G= , CM000668.2:g.14133900G= GRCh38
NC_000006.11:g.14134131G= , CM000668.1:g.14134131G= GRCh37
NC_000006.10:g.14242110G= NCBI36
NG_030372.1:g.21645G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379153.4:c.489+145G= MANE Select ENSP00000368450.3:n.489+145G=
ENST00000379153.3:c.489+145G= ENSP00000368450.3:n.489+145G=
ENST00000612003.4:c.312+145G= ENSP00000480760.1:n.312+145G=
NM_001040280.1:c.489+145G= NP_001035370.1:n.489+145G=
NM_001251901.1:c.312+145G= NP_001238830.1:n.312+145G=
NM_004233.3:c.489+145G= NP_004224.1:n.489+145G=
NM_004233.4:c.489+145G= MANE Select NP_004224.1:n.489+145G=
NM_001040280.2:c.489+145G= NP_001035370.1:n.489+145G=
NM_001040280.3:c.489+145G= NP_001035370.1:n.489+145G=
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