Canonical Allele Identifier: CA127253425
Gene: RAD50 HGNC NCBI

Linked Data

dbSNP Id: rs972781662

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132556909A>G , CM000667.2:g.132556909A>G GRCh38
NC_000005.9:g.131892601A>G , CM000667.1:g.131892601A>G GRCh37
NC_000005.8:g.131920500A>G NCBI36
NG_021151.1:g.4986A>G
NG_021151.2:g.4933A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-168-2375A>G ENSP00000492349.2:n.-168-2375A>G
ENST00000638504.1:n.207-2375A>G
ENST00000638568.2:c.-169+436A>G ENSP00000491158.2:n.-169+436A>G
ENST00000639899.1:n.290-2375A>G
ENST00000640655.2:c.-168-2375A>G ENSP00000491596.2:n.-168-2375A>G
ENST00000416135.5:c.-169+436A>G ENSP00000389515.1:n.-169+436A>G