HGVS | Genome Assembly |
---|---|
NC_000017.11:g.8086002T>C , CM000679.2:g.8086002T>C | GRCh38 |
NC_000017.10:g.7989320T>C , CM000679.1:g.7989320T>C | GRCh37 |
NC_000017.9:g.7930045T>C | NCBI36 |
NG_007099.1:g.6702A>G | |
NG_007099.2:g.6715A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647874.1:c.352+14A>G MANE Select | ENSP00000497784.1:n.352+14A>G | |
ENST00000319144.4:c.352+14A>G | ENSP00000315167.4:n.352+14A>G | |
NM_001139.2:c.352+14A>G | NP_001130.1:n.352+14A>G | |
NM_001139.3:c.352+14A>G MANE Select | NP_001130.1:n.352+14A>G |