Canonical Allele Identifier: CA2675215480
Gene: RAD50 HGNC NCBI

Linked Data

gnomAD v4: 5-132556952-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132556952T>A , CM000667.2:g.132556952T>A GRCh38
NC_000005.9:g.131892644T>A , CM000667.1:g.131892644T>A GRCh37
NC_000005.8:g.131920543T>A NCBI36
NG_021151.1:g.5029T>A
NG_021151.2:g.4976T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-168-2332T>A ENSP00000492349.2:n.-168-2332T>A
ENST00000638504.1:n.207-2332T>A
ENST00000638568.2:c.-169+479T>A ENSP00000491158.2:n.-169+479T>A
ENST00000639899.1:n.290-2332T>A
ENST00000640655.2:c.-168-2332T>A ENSP00000491596.2:n.-168-2332T>A
ENST00000651541.1:c.-226T>A ENSP00000498795.1:n.-226T>A
ENST00000378823.7:c.-373T>A ENSP00000368100.4:n.-373T>A
ENST00000416135.5:c.-169+479T>A ENSP00000389515.1:n.-169+479T>A
ENST00000533482.5:c.-373T>A ENSP00000431225.1:n.-373T>A
NM_005732.3:c.-373T>A NP_005723.2:n.-373T>A
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