HGVS | Genome Assembly |
---|---|
NC_000017.11:g.16948948A>G , CM000679.2:g.16948948A>G | GRCh38 |
NC_000017.10:g.16852262A>G , CM000679.1:g.16852262A>G | GRCh37 |
NC_000017.9:g.16792987A>G | NCBI36 |
NG_007281.1:g.28141T>C , LRG_120:g.28141T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261652.7:c.235T>C MANE Select | ENSP00000261652.2:p.Tyr79His | |
ENST00000261652.6:c.235T>C | ENSP00000261652.2:p.Tyr79His | |
ENST00000579315.5:c.235T>C | ENSP00000464069.1:p.Tyr79His | |
ENST00000581616.2:n.238T>C | ||
ENST00000582931.5:n.139T>C | ||
ENST00000583789.1:c.97T>C | ENSP00000462952.1:p.Tyr33His | |
ENST00000584950.5:c.97T>C | ENSP00000463582.1:p.Tyr33His | |
NM_012452.2:c.235T>C , LRG_120t1:c.235T>C | NP_036584.1:p.Tyr79His | |
NM_012452.3:c.235T>C MANE Select | NP_036584.1:p.Tyr79His |