HGVS | Genome Assembly |
---|---|
NC_000017.11:g.8086051T>G , CM000679.2:g.8086051T>G | GRCh38 |
NC_000017.10:g.7989369T>G , CM000679.1:g.7989369T>G | GRCh37 |
NC_000017.9:g.7930094T>G | NCBI36 |
NG_007099.1:g.6653A>C | |
NG_007099.2:g.6666A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647874.1:c.317A>C MANE Select | ENSP00000497784.1:p.Asp106Ala | |
ENST00000319144.4:c.317A>C | ENSP00000315167.4:p.Asp106Ala | |
NM_001139.2:c.317A>C | NP_001130.1:p.Asp106Ala | |
NM_001139.3:c.317A>C MANE Select | NP_001130.1:p.Asp106Ala |