Canonical Allele Identifier: CA135105517

Gene: CD83

Linked Data

• dbSNP Id: rs1010652302
• gnomAD v2: 6-14134085-A-C
• gnomAD v3: 6-14133854-A-C
• gnomAD v4: 6-14133854-A-C
• MyVariant Identifiers: chr6:g.14134085A>C (hg19) ; chr6:g.14133854A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.14133854A>C , CM000668.2:g.14133854A>C	GRCh38
NC_000006.11:g.14134085A>C , CM000668.1:g.14134085A>C	GRCh37
NC_000006.10:g.14242064A>C	NCBI36
NG_030372.1:g.21599A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379153.4:c.489+99A>C MANE Select	ENSP00000368450.3:n.489+99A>C
ENST00000379153.3:c.489+99A>C	ENSP00000368450.3:n.489+99A>C
ENST00000612003.4:c.312+99A>C	ENSP00000480760.1:n.312+99A>C
NM_001040280.1:c.489+99A>C	NP_001035370.1:n.489+99A>C
NM_001251901.1:c.312+99A>C	NP_001238830.1:n.312+99A>C
NM_004233.3:c.489+99A>C	NP_004224.1:n.489+99A>C
NM_004233.4:c.489+99A>C MANE Select	NP_004224.1:n.489+99A>C
NM_001040280.2:c.489+99A>C	NP_001035370.1:n.489+99A>C
NM_001040280.3:c.489+99A>C	NP_001035370.1:n.489+99A>C