Canonical Allele Identifier: CA2675215417
Gene: RAD50 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132556916G>A , CM000667.2:g.132556916G>A GRCh38
NC_000005.9:g.131892608G>A , CM000667.1:g.131892608G>A GRCh37
NC_000005.8:g.131920507G>A NCBI36
NG_021151.1:g.4993G>A
NG_021151.2:g.4940G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-168-2368G>A ENSP00000492349.2:n.-168-2368G>A
ENST00000638504.1:n.207-2368G>A
ENST00000638568.2:c.-169+443G>A ENSP00000491158.2:n.-169+443G>A
ENST00000639899.1:n.290-2368G>A
ENST00000640655.2:c.-168-2368G>A ENSP00000491596.2:n.-168-2368G>A
ENST00000416135.5:c.-169+443G>A ENSP00000389515.1:n.-169+443G>A