HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6714188A>G , CM000681.2:g.6714188A>G | GRCh38 |
NC_000019.9:g.6714199A>G , CM000681.1:g.6714199A>G | GRCh37 |
NC_000019.8:g.6665199A>G | NCBI36 |
NG_009557.1:g.11464T>C , LRG_27:g.11464T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.537T>C | ENSP00000512083.1:p.Thr179= | |
ENST00000245907.11:c.660T>C MANE Select | ENSP00000245907.4:p.Thr220= | |
ENST00000245907.10:c.660T>C | ENSP00000245907.4:p.Thr220= | |
ENST00000595577.1:n.164T>C | ||
NM_000064.3:c.660T>C | NP_000055.2:p.Thr220= | |
NM_000064.4:c.660T>C MANE Select | NP_000055.2:p.Thr220= |