HGVS | Genome Assembly |
---|---|
NC_000002.12:g.21001865T>C , CM000664.2:g.21001865T>C | GRCh38 |
NC_000002.11:g.21224737T>C , CM000664.1:g.21224737T>C | GRCh37 |
NC_000002.10:g.21078242T>C | NCBI36 |
NG_011793.1:g.47209A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000233242.5:c.13557A>G MANE Select | ENSP00000233242.1:p.Arg4519= | |
ENST00000616098.4:c.13555A>G | ENSP00000477990.1:n.13555A>G | |
NM_000384.2:c.13557A>G | NP_000375.2:p.Arg4519= | |
XM_011532809.1:c.5870-2592A>G | XP_011531111.1:n.5870-2592A>G | |
NM_000384.3:c.13557A>G MANE Select | NP_000375.3:p.Arg4519= |