HGVS | Genome Assembly |
---|---|
NC_000010.11:g.1410521_1410522del , CM000672.2:g.1410521_1410522del | GRCh38 |
NC_000010.10:g.1452716_1452717del , CM000672.1:g.1452716_1452717del | GRCh37 |
NC_000010.9:g.1442716_1442717del | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000381312.6:c.101-31359_101-31358del MANE Select | ENSP00000370713.1:n.101-31359_101-31358de... | |
ENST00000381312.5:c.101-31359_101-31358del | ENSP00000370713.1:n.101-31359_101-31358de... | |
NM_018702.3:c.101-31359_101-31358del | NP_061172.1:n.101-31359_101-31358del | |
XR_930468.1:n.449-31359_449-31358del | ||
NM_018702.4:c.101-31359_101-31358del MANE Select | NP_061172.1:n.101-31359_101-31358del |