Canonical Allele Identifier: CA2677392559
Gene: CD83 HGNC NCBI

Linked Data

gnomAD v4: 6-14133863-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.14133863A>G , CM000668.2:g.14133863A>G GRCh38
NC_000006.11:g.14134094A>G , CM000668.1:g.14134094A>G GRCh37
NC_000006.10:g.14242073A>G NCBI36
NG_030372.1:g.21608A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000379153.4:c.489+108A>G MANE Select ENSP00000368450.3:n.489+108A>G
ENST00000379153.3:c.489+108A>G ENSP00000368450.3:n.489+108A>G
ENST00000612003.4:c.312+108A>G ENSP00000480760.1:n.312+108A>G
NM_001040280.1:c.489+108A>G NP_001035370.1:n.489+108A>G
NM_001251901.1:c.312+108A>G NP_001238830.1:n.312+108A>G
NM_004233.3:c.489+108A>G NP_004224.1:n.489+108A>G
NM_004233.4:c.489+108A>G MANE Select NP_004224.1:n.489+108A>G
NM_001040280.2:c.489+108A>G NP_001035370.1:n.489+108A>G
NM_001040280.3:c.489+108A>G NP_001035370.1:n.489+108A>G
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