HGVS | Genome Assembly |
---|---|
NC_000019.10:g.9126938T>A , CM000681.2:g.9126938T>A | GRCh38 |
NC_000019.9:g.9237614T>A , CM000681.1:g.9237614T>A | GRCh37 |
NC_000019.8:g.9098614T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000305444.2:c.13A>T MANE Select | ENSP00000302867.2:p.Asn5Tyr | |
NM_001001958.1:c.13A>T MANE Select | NP_001001958.1:p.Asn5Tyr |