HGVS | Genome Assembly |
---|---|
NC_000019.10:g.35849618A= , CM000681.2:g.35849618A= | GRCh38 |
NC_000019.9:g.36340520A= , CM000681.1:g.36340520A= | GRCh37 |
NC_000019.8:g.41032360A= | NCBI36 |
NG_013356.2:g.24670T= , LRG_693:g.24670T= | |
NG_051206.1:g.2984A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378910.10:c.644T= MANE Select | ENSP00000368190.4:p.Leu215= | |
ENST00000353632.6:c.644T= | ENSP00000343634.5:p.Leu215= | |
ENST00000378910.9:c.644T= | ENSP00000368190.4:p.Leu215= | |
NM_004646.3:c.644T= , LRG_693t1:c.644T= | NP_004637.1:p.Leu215= | |
NM_004646.4:c.644T= MANE Select | NP_004637.1:p.Leu215= |