HGVS | Genome Assembly |
---|---|
NC_000002.12:g.21002180C>A , CM000664.2:g.21002180C>A | GRCh38 |
NC_000002.11:g.21225052C>A , CM000664.1:g.21225052C>A | GRCh37 |
NC_000002.10:g.21078557C>A | NCBI36 |
NG_011793.1:g.46894G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000233242.5:c.13242G>T MANE Select | ENSP00000233242.1:p.Leu4414= | |
ENST00000616098.4:c.13240G>T | ENSP00000477990.1:n.13240G>T | |
NM_000384.2:c.13242G>T | NP_000375.2:p.Leu4414= | |
XM_011532809.1:c.5870-2907G>T | XP_011531111.1:n.5870-2907G>T | |
NM_000384.3:c.13242G>T MANE Select | NP_000375.3:p.Leu4414= |