HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6713315T>G , CM000681.2:g.6713315T>G | GRCh38 |
NC_000019.9:g.6713326T>G , CM000681.1:g.6713326T>G | GRCh37 |
NC_000019.8:g.6664326T>G | NCBI36 |
NG_009557.1:g.12337A>C , LRG_27:g.12337A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.754A>C | ENSP00000512083.1:p.Ile252Leu | |
ENST00000695654.1:c.1A>C | ENSP00000512085.1:p.Ile1Leu | |
ENST00000695692.1:n.201A>C | ||
ENST00000245907.11:c.877A>C MANE Select | ENSP00000245907.4:p.Ile293Leu | |
ENST00000245907.10:c.877A>C | ENSP00000245907.4:p.Ile293Leu | |
ENST00000594270.5:n.1A>C | ||
ENST00000595577.1:n.381A>C | ||
ENST00000597442.5:n.127A>C | ||
NM_000064.3:c.877A>C | NP_000055.2:p.Ile293Leu | |
NM_000064.4:c.877A>C MANE Select | NP_000055.2:p.Ile293Leu |