HGVS | Genome Assembly |
---|---|
NC_000021.9:g.31667281T= , CM000683.2:g.31667281T= | GRCh38 |
NC_000021.8:g.33039594T= , CM000683.1:g.33039594T= | GRCh37 |
NC_000021.7:g.31961465T= | NCBI36 |
NG_008689.1:g.12660T= , LRG_652:g.12660T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270142.11:c.263T= MANE Select | ENSP00000270142.7:p.Val88= | |
ENST00000270142.10:c.263T= | ENSP00000270142.6:p.Val88= | |
ENST00000389995.4:c.206T= | ENSP00000374645.4:p.Val69= | |
ENST00000470944.1:n.1191T= | ||
ENST00000476106.5:n.526T= | ||
NM_000454.4:c.263T= , LRG_652t1:c.263T= | NP_000445.1:p.Val88= | |
NM_000454.5:c.263T= MANE Select | NP_000445.1:p.Val88= |