HGVS | Genome Assembly |
---|---|
NC_000009.12:g.129814126C>A , CM000671.2:g.129814126C>A | GRCh38 |
NC_000009.11:g.132576405C>A , CM000671.1:g.132576405C>A | GRCh37 |
NC_000009.10:g.131616226C>A | NCBI36 |
NG_008049.1:g.15037G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000351698.5:c.845G>T MANE Select | ENSP00000345719.4:p.Arg282Leu | |
ENST00000651202.1:c.*113G>T | ENSP00000498222.1:n.*113G>T | |
ENST00000351698.4:c.845G>T | ENSP00000345719.4:p.Arg282Leu | |
ENST00000474192.1:n.429G>T | ||
NM_000113.2:c.845G>T | NP_000104.1:p.Arg282Leu | |
XR_929731.1:n.1172G>T | ||
XR_929731.3:n.1040G>T | ||
NM_000113.3:c.845G>T MANE Select | NP_000104.1:p.Arg282Leu |