HGVS | Genome Assembly |
---|---|
NC_000002.12:g.96143585_96143593del , CM000664.2:g.96143585_96143593del | GRCh38 |
NC_000002.11:g.96809324_96809332del , CM000664.1:g.96809324_96809332del | GRCh37 |
NC_000002.10:g.96173051_96173059del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000288943.5:c.*230_*238del MANE Select | ENSP00000288943.4:n.*230_*238del | |
ENST00000288943.4:c.*230_*238del | ENSP00000288943.4:n.*230_*238del | |
NM_004418.3:c.*230_*238del | NP_004409.1:n.*230_*238del | |
XM_017003546.1:c.*230_*238del | XP_016859035.1:n.*230_*238del | |
NM_004418.4:c.*230_*238del MANE Select | NP_004409.1:n.*230_*238del |