Canonical Allele Identifier: CA1611669840
Gene: CD83 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.14133853G= , CM000668.2:g.14133853G= GRCh38
NC_000006.11:g.14134084G= , CM000668.1:g.14134084G= GRCh37
NC_000006.10:g.14242063G= NCBI36
NG_030372.1:g.21598G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379153.4:c.489+98G= MANE Select ENSP00000368450.3:n.489+98G=
ENST00000379153.3:c.489+98G= ENSP00000368450.3:n.489+98G=
ENST00000612003.4:c.312+98G= ENSP00000480760.1:n.312+98G=
NM_001040280.1:c.489+98G= NP_001035370.1:n.489+98G=
NM_001251901.1:c.312+98G= NP_001238830.1:n.312+98G=
NM_004233.3:c.489+98G= NP_004224.1:n.489+98G=
NM_004233.4:c.489+98G= MANE Select NP_004224.1:n.489+98G=
NM_001040280.2:c.489+98G= NP_001035370.1:n.489+98G=
NM_001040280.3:c.489+98G= NP_001035370.1:n.489+98G=