Canonical Allele Identifier: CA2677392545
Gene: CD83 HGNC NCBI

Linked Data

gnomAD v4: 6-14133853-G-T
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Genomic Alleles

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

Transcript Alleles

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