Canonical Allele Identifier: CA1081647708
Gene: RAD50 HGNC NCBI

Linked Data

dbSNP Id: rs1750000645

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132556941G>A , CM000667.2:g.132556941G>A GRCh38
NC_000005.9:g.131892633G>A , CM000667.1:g.131892633G>A GRCh37
NC_000005.8:g.131920532G>A NCBI36
NG_021151.1:g.5018G>A
NG_021151.2:g.4965G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-168-2343G>A ENSP00000492349.2:n.-168-2343G>A
ENST00000638504.1:n.207-2343G>A
ENST00000638568.2:c.-169+468G>A ENSP00000491158.2:n.-169+468G>A
ENST00000639899.1:n.290-2343G>A
ENST00000640655.2:c.-168-2343G>A ENSP00000491596.2:n.-168-2343G>A
ENST00000651541.1:c.-237G>A ENSP00000498795.1:n.-237G>A
ENST00000378823.7:c.-384G>A ENSP00000368100.4:n.-384G>A
ENST00000416135.5:c.-169+468G>A ENSP00000389515.1:n.-169+468G>A
ENST00000533482.5:c.-384G>A ENSP00000431225.1:n.-384G>A
NM_005732.3:c.-384G>A NP_005723.2:n.-384G>A