HGVS | Genome Assembly |
---|---|
NC_000001.11:g.215675299T>G , CM000663.2:g.215675299T>G | GRCh38 |
NC_000001.10:g.215848641T>G , CM000663.1:g.215848641T>G | GRCh37 |
NC_000001.9:g.213915264T>G | NCBI36 |
NG_009497.2:g.753150A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.12612A>C MANE Select | ENSP00000305941.3:p.Thr4204= | |
ENST00000674083.1:c.12612A>C | ENSP00000501296.1:p.Thr4204= | |
ENST00000307340.7:c.12612A>C | ENSP00000305941.3:p.Thr4204= | |
NM_206933.4:c.12612A>C MANE Select | NP_996816.3:p.Thr4204= |