HGVS | Genome Assembly |
---|---|
NC_000010.11:g.1410754_1410757del , CM000672.2:g.1410754_1410757del | GRCh38 |
NC_000010.10:g.1452949_1452952del , CM000672.1:g.1452949_1452952del | GRCh37 |
NC_000010.9:g.1442949_1442952del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381312.6:c.101-31597_101-31594del MANE Select | ENSP00000370713.1:n.101-31597_101-31594del | |
ENST00000381312.5:c.101-31597_101-31594del | ENSP00000370713.1:n.101-31597_101-31594del | |
NM_018702.3:c.101-31597_101-31594del | NP_061172.1:n.101-31597_101-31594del | |
XR_930468.1:n.449-31597_449-31594del | ||
NM_018702.4:c.101-31597_101-31594del MANE Select | NP_061172.1:n.101-31597_101-31594del |