HGVS | Genome Assembly |
---|---|
NC_000005.10:g.128357287A>G , CM000667.2:g.128357287A>G | GRCh38 |
NC_000005.9:g.127692979A>G , CM000667.1:g.127692979A>G | GRCh37 |
NC_000005.8:g.127720878A>G | NCBI36 |
NG_008750.1:g.185757T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000262464.9:c.2663T>C MANE Select | ENSP00000262464.4:p.Leu888Ser | |
ENST00000262464.8:c.2663T>C | ENSP00000262464.4:p.Leu888Ser | |
ENST00000508053.5:c.2663T>C | ENSP00000424571.1:p.Leu888Ser | |
ENST00000508989.5:c.2564T>C | ENSP00000425596.1:p.Leu855Ser | |
ENST00000619499.4:c.2660T>C | ENSP00000482132.1:p.Leu887Ser | |
NM_001999.3:c.2663T>C | NP_001990.2:p.Leu888Ser | |
XM_017009228.2:c.2510T>C | XP_016864717.1:p.Leu837Ser | |
NM_001999.4:c.2663T>C MANE Select | NP_001990.2:p.Leu888Ser |