HGVS | Genome Assembly |
---|---|
NC_000002.12:g.21010394A>G , CM000664.2:g.21010394A>G | GRCh38 |
NC_000002.11:g.21233266A>G , CM000664.1:g.21233266A>G | GRCh37 |
NC_000002.10:g.21086771A>G | NCBI36 |
NG_011793.1:g.38680T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000233242.5:c.6474T>C MANE Select | ENSP00000233242.1:p.Ile2158= | |
ENST00000616098.4:c.6474T>C | ENSP00000477990.1:p.Ile2158= | |
NM_000384.2:c.6474T>C | NP_000375.2:p.Ile2158= | |
XM_011532809.1:c.5869+339T>C | XP_011531111.1:n.5869+339T>C | |
NM_000384.3:c.6474T>C MANE Select | NP_000375.3:p.Ile2158= |