HGVS | Genome Assembly |
---|---|
NC_000010.11:g.104037693T>C , CM000672.2:g.104037693T>C | GRCh38 |
NC_000010.10:g.105797451T>C , CM000672.1:g.105797451T>C | GRCh37 |
NC_000010.9:g.105787441T>C | NCBI36 |
NG_007069.1:g.53188A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369733.8:c.3016A>G | ENSP00000358748.3:p.Thr1006Ala | |
ENST00000648076.2:c.3151A>G MANE Select | ENSP00000497653.1:p.Thr1051Ala | |
ENST00000353479.9:c.3151A>G | ENSP00000340937.5:p.Thr1051Ala | |
ENST00000369733.7:c.3016A>G | ENSP00000358748.3:p.Thr1006Ala | |
NM_000494.3:c.3151A>G | NP_000485.3:p.Thr1051Ala | |
NM_000494.4:c.3151A>G MANE Select | NP_000485.3:p.Thr1051Ala |