Canonical Allele Identifier: CA135105516
Gene: CD83 HGNC NCBI

Linked Data

dbSNP Id: rs767790679
gnomAD v3: 6-14133853-G-A
gnomAD v4: 6-14133853-G-A

Genomic Alleles

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

Transcript Alleles

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