Canonical Allele Identifier: CA2635877631
Gene: CD68 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7581498dup , CM000679.2:g.7581498dup GRCh38
NC_000017.10:g.7484816dup , CM000679.1:g.7484816dup GRCh37
NC_000017.9:g.7425540dup NCBI36
NG_009204.1:g.2852dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000250092.11:c.1052dup MANE Select ENSP00000250092.6:p.Tyr351Ter
ENST00000250092.10:c.1052dup ENSP00000250092.6:p.Tyr351Ter
ENST00000380498.10:c.971dup ENSP00000369867.6:p.Tyr324Ter
ENST00000584180.1:c.767dup
NM_001040059.1:c.971dup NP_001035148.1:p.Tyr324Ter
NM_001251.2:c.1052dup NP_001242.2:p.Tyr351Ter
NM_001251.3:c.1052dup MANE Select NP_001242.2:p.Tyr351Ter
NM_001040059.2:c.971dup NP_001035148.1:p.Tyr324Ter