HGVS | Genome Assembly |
---|---|
NC_000023.11:g.38367318G>T , CM000685.2:g.38367318G>T | GRCh38 |
NC_000023.10:g.38226571G>T , CM000685.1:g.38226571G>T | GRCh37 |
NC_000023.9:g.38111515G>T | NCBI36 |
NG_008471.1:g.19836G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000039007.5:c.105G>T MANE Select | ENSP00000039007.4:p.Val35= | |
ENST00000643344.1:c.105G>T | ENSP00000496606.1:p.Val35= | |
ENST00000039007.4:c.105G>T | ENSP00000039007.4:p.Val35= | |
ENST00000465127.1:c.172-298803G>T | ENSP00000417050.1:n.172-298803G>T | |
ENST00000488812.1:n.197G>T | ||
NM_000531.5:c.105G>T | NP_000522.3:p.Val35= | |
XM_017029556.1:c.105G>T | XP_016885045.1:p.Val35= | |
NM_000531.6:c.105G>T MANE Select | NP_000522.3:p.Val35= |