HGVS | Genome Assembly |
---|---|
NC_000010.11:g.104038411A>C , CM000672.2:g.104038411A>C | GRCh38 |
NC_000010.10:g.105798169A>C , CM000672.1:g.105798169A>C | GRCh37 |
NC_000010.9:g.105788159A>C | NCBI36 |
NG_007069.1:g.52470T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369733.8:c.2930T>G | ENSP00000358748.3:p.Met977Arg | |
ENST00000648076.2:c.3065T>G MANE Select | ENSP00000497653.1:p.Met1022Arg | |
ENST00000353479.9:c.3065T>G | ENSP00000340937.5:p.Met1022Arg | |
ENST00000369733.7:c.2930T>G | ENSP00000358748.3:p.Met977Arg | |
NM_000494.3:c.3065T>G | NP_000485.3:p.Met1022Arg | |
NM_000494.4:c.3065T>G MANE Select | NP_000485.3:p.Met1022Arg |