Canonical Allele Identifier: CA2768437547
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132556915G>T , CM000667.2:g.132556915G>T GRCh38
NC_000005.9:g.131892607G>T , CM000667.1:g.131892607G>T GRCh37
NC_000005.8:g.131920506G>T NCBI36
NG_021151.1:g.4992G>T
NG_021151.2:g.4939G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-168-2369G>T ENSP00000492349.2:n.-168-2369G>T
ENST00000638504.1:n.207-2369G>T
ENST00000638568.2:c.-169+442G>T ENSP00000491158.2:n.-169+442G>T
ENST00000639899.1:n.290-2369G>T
ENST00000640655.2:c.-168-2369G>T ENSP00000491596.2:n.-168-2369G>T
ENST00000416135.5:c.-169+442G>T ENSP00000389515.1:n.-169+442G>T