HGVS | Genome Assembly |
---|---|
NC_000016.10:g.1351964_1351974del , CM000678.2:g.1351964_1351974del | GRCh38 |
NC_000016.9:g.1401965_1401975del , CM000678.1:g.1401965_1401975del | GRCh37 |
NC_000016.8:g.1341966_1341976del | NCBI36 |
NG_016985.1:g.5066_5076del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000527168.6:n.19_29del | ||
ENST00000683366.1:c.-2_9del | ||
ENST00000683887.1:c.-2_9del | ||
ENST00000204679.9:c.-2_9del | ||
ENST00000204679.8:c.-2_9del | ||
ENST00000526820.5:c.-2_9del | ||
ENST00000527137.2:c.-2_9del | ||
ENST00000527168.5:n.11_21del | ||
ENST00000527876.5:c.-2_9del | ||
ENST00000529957.5:n.19_29del | ||
ENST00000534197.5:n.17_27del | ||
NM_032520.4:c.-2_9del | ||
XM_017023782.1:c.-2_9del | ||
NM_032520.5:c.-2_9del |