HGVS | Genome Assembly |
---|---|
NC_000002.12:g.21002756C>A , CM000664.2:g.21002756C>A | GRCh38 |
NC_000002.11:g.21225628C>A , CM000664.1:g.21225628C>A | GRCh37 |
NC_000002.10:g.21079133C>A | NCBI36 |
NG_011793.1:g.46318G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000233242.5:c.12666G>T MANE Select | ENSP00000233242.1:p.Arg4222Ser | |
ENST00000616098.4:c.12666G>T | ENSP00000477990.1:p.Arg4222Ser | |
NM_000384.2:c.12666G>T | NP_000375.2:p.Arg4222Ser | |
XM_011532809.1:c.5870-3483G>T | XP_011531111.1:n.5870-3483G>T | |
NM_000384.3:c.12666G>T MANE Select | NP_000375.3:p.Arg4222Ser |