HGVS | Genome Assembly |
---|---|
NC_000010.11:g.104038413G>T , CM000672.2:g.104038413G>T | GRCh38 |
NC_000010.10:g.105798171G>T , CM000672.1:g.105798171G>T | GRCh37 |
NC_000010.9:g.105788161G>T | NCBI36 |
NG_007069.1:g.52468C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369733.8:c.2928C>A | ENSP00000358748.3:p.Tyr976Ter | |
ENST00000648076.2:c.3063C>A MANE Select | ENSP00000497653.1:p.Tyr1021Ter | |
ENST00000353479.9:c.3063C>A | ENSP00000340937.5:p.Tyr1021Ter | |
ENST00000369733.7:c.2928C>A | ENSP00000358748.3:p.Tyr976Ter | |
NM_000494.3:c.3063C>A | NP_000485.3:p.Tyr1021Ter | |
NM_000494.4:c.3063C>A MANE Select | NP_000485.3:p.Tyr1021Ter |