HGVS | Genome Assembly |
---|---|
NC_000002.12:g.96143593_96143594insTA , CM000664.2:g.96143593_96143594insTA | GRCh38 |
NC_000002.11:g.96809332_96809333insTA , CM000664.1:g.96809332_96809333insTA | GRCh37 |
NC_000002.10:g.96173059_96173060insTA | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000288943.5:c.*229_*230insTA MANE Select | ENSP00000288943.4:n.*229_*230insTA | |
ENST00000288943.4:c.*229_*230insTA | ENSP00000288943.4:n.*229_*230insTA | |
NM_004418.3:c.*229_*230insTA | NP_004409.1:n.*229_*230insTA | |
XM_017003546.1:c.*229_*230insTA | XP_016859035.1:n.*229_*230insTA | |
NM_004418.4:c.*229_*230insTA MANE Select | NP_004409.1:n.*229_*230insTA |