HGVS | Genome Assembly |
---|---|
NC_000005.10:g.147831543A>T , CM000667.2:g.147831543A>T | GRCh38 |
NC_000005.9:g.147211106A>T , CM000667.1:g.147211106A>T | GRCh37 |
NC_000005.8:g.147191299A>T | NCBI36 |
NG_008356.2:g.12689T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000296695.10:c.35T>A MANE Select | ENSP00000296695.5:p.Leu12Ter | |
ENST00000296695.9:c.35T>A | ENSP00000296695.5:p.Leu12Ter | |
ENST00000510027.2:c.35T>A | ENSP00000427376.1:p.Leu12Ter | |
NM_003122.4:c.35T>A | NP_003113.2:p.Leu12Ter | |
NM_001354966.1:c.35T>A | NP_001341895.1:p.Leu12Ter | |
NM_001354966.2:c.35T>A | NP_001341895.1:p.Leu12Ter | |
NM_001379610.1:c.35T>A MANE Select | NP_001366539.1:p.Leu12Ter | |
NM_003122.5:c.35T>A | NP_003113.2:p.Leu12Ter |