Canonical Allele Identifier: CA2675215507
Gene: RAD50 HGNC NCBI

Linked Data

dbSNP Id: rs2149829720

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132556969A>G , CM000667.2:g.132556969A>G GRCh38
NC_000005.9:g.131892661A>G , CM000667.1:g.131892661A>G GRCh37
NC_000005.8:g.131920560A>G NCBI36
NG_021151.1:g.5046A>G
NG_021151.2:g.4993A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-168-2315A>G ENSP00000492349.2:n.-168-2315A>G
ENST00000638504.1:n.207-2315A>G
ENST00000638568.2:c.-169+496A>G ENSP00000491158.2:n.-169+496A>G
ENST00000639899.1:n.290-2315A>G
ENST00000640655.2:c.-168-2315A>G ENSP00000491596.2:n.-168-2315A>G
ENST00000651541.1:c.-209A>G ENSP00000498795.1:n.-209A>G
ENST00000378823.7:c.-356A>G ENSP00000368100.4:n.-356A>G
ENST00000416135.5:c.-169+496A>G ENSP00000389515.1:n.-169+496A>G
ENST00000533482.5:c.-356A>G ENSP00000431225.1:n.-356A>G
NM_005732.3:c.-356A>G NP_005723.2:n.-356A>G