HGVS | Genome Assembly |
---|---|
NC_000019.10:g.9126466A>G , CM000681.2:g.9126466A>G | GRCh38 |
NC_000019.9:g.9237142A>G , CM000681.1:g.9237142A>G | GRCh37 |
NC_000019.8:g.9098142A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000305444.2:c.485T>C MANE Select | ENSP00000302867.2:p.Met162Thr | |
NM_001001958.1:c.485T>C MANE Select | NP_001001958.1:p.Met162Thr |