HGVS | Genome Assembly |
---|---|
NC_000017.11:g.8012275T>C , CM000679.2:g.8012275T>C | GRCh38 |
NC_000017.10:g.7915593T>C , CM000679.1:g.7915593T>C | GRCh37 |
NC_000017.9:g.7856318T>C | NCBI36 |
NG_009092.1:g.14606T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000254854.5:c.1881T>C MANE Select | ENSP00000254854.4:p.Leu627= | |
ENST00000254854.4:c.1881T>C | ENSP00000254854.4:p.Leu627= | |
NM_000180.3:c.1881T>C | NP_000171.1:p.Leu627= | |
XM_011523816.1:c.1881T>C | XP_011522118.1:p.Leu627= | |
NM_000180.4:c.1881T>C MANE Select | NP_000171.1:p.Leu627= |