HGVS | Genome Assembly |
---|---|
NC_000017.11:g.16948947T>A , CM000679.2:g.16948947T>A | GRCh38 |
NC_000017.10:g.16852261T>A , CM000679.1:g.16852261T>A | GRCh37 |
NC_000017.9:g.16792986T>A | NCBI36 |
NG_007281.1:g.28142A>T , LRG_120:g.28142A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261652.7:c.236A>T MANE Select | ENSP00000261652.2:p.Tyr79Phe | |
ENST00000261652.6:c.236A>T | ENSP00000261652.2:p.Tyr79Phe | |
ENST00000579315.5:c.236A>T | ENSP00000464069.1:p.Tyr79Phe | |
ENST00000581616.2:n.239A>T | ||
ENST00000582931.5:n.140A>T | ||
ENST00000583789.1:c.98A>T | ENSP00000462952.1:p.Tyr33Phe | |
ENST00000584950.5:c.98A>T | ENSP00000463582.1:p.Tyr33Phe | |
NM_012452.2:c.236A>T , LRG_120t1:c.236A>T | NP_036584.1:p.Tyr79Phe | |
NM_012452.3:c.236A>T MANE Select | NP_036584.1:p.Tyr79Phe |