Canonical Allele Identifier: CA226546664
Gene: ANKRD49 HGNC NCBI
MRE11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94493959C>T , CM000673.2:g.94493959C>T GRCh38
NC_000011.9:g.94227125C>T , CM000673.1:g.94227125C>T GRCh37
NC_000011.8:g.93866773C>T NCBI36
NG_007261.1:g.4916G>A , LRG_85:g.4916G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000544612.5:c.-167C>T (ANKRD49) ENSP00000440396.1:n.-167C>T
XM_011542837.1:c.-105-1053G>A (MRE11) XP_011541139.1:n.-105-1053G>A
XM_011542837.2:c.-105-1053G>A (MRE11) XP_011541139.1:n.-105-1053G>A