HGVS | Genome Assembly |
---|---|
NC_000023.11:g.85963667_85964054del , CM000685.2:g.85963667_85964054del | GRCh38 |
NC_000023.10:g.85218672_85219059del , CM000685.1:g.85218672_85219059del | GRCh37 |
NC_000023.9:g.85105328_85105715del | NCBI36 |
NG_009874.2:g.88511_88898del , LRG_699:g.88511_88898del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000357749.7:c.315_702del | ||
ENST00000357749.6:c.315_702del | ||
ENST00000467744.2:n.126+63439_126+63826del | ||
NM_000390.2:c.315_702del , LRG_699t1:c.315_702del | ||
XM_006724615.2:c.252_639del | ||
XM_011530839.1:c.-130_258del | ||
NM_000390.3:c.315_702del | ||
NM_001320959.1:c.-130_258del | ||
NM_001362517.1:c.-130_258del | ||
NM_001362518.1:c.-126-4_258del | ||
NM_001362519.1:c.-126-4_258del | ||
XM_017029242.2:c.315_702del | ||
XM_017029246.1:c.-126-4_258del | ||
XM_024452331.1:c.-130_258del | ||
NM_000390.4:c.315_702del | ||
NM_001362518.2:c.-126-4_258del |