HGVS | Genome Assembly |
---|---|
NC_000011.10:g.22624990T>C , CM000673.2:g.22624990T>C | GRCh38 |
NC_000011.9:g.22646536T>C , CM000673.1:g.22646536T>C | GRCh37 |
NC_000011.8:g.22603112T>C | NCBI36 |
NG_007425.1:g.5852A>G , LRG_527:g.5852A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327470.6:c.821A>G MANE Select | ENSP00000330875.3:p.Tyr274Cys | |
ENST00000327470.4:c.821A>G | ENSP00000330875.3:p.Tyr274Cys | |
NM_022725.3:c.821A>G , LRG_527t1:c.821A>G | NP_073562.1:p.Tyr274Cys | |
NM_022725.4:c.821A>G MANE Select | NP_073562.1:p.Tyr274Cys |