HGVS | Genome Assembly |
---|---|
NC_000023.11:g.38370218A>T , CM000685.2:g.38370218A>T | GRCh38 |
NC_000023.10:g.38229471A>T , CM000685.1:g.38229471A>T | GRCh37 |
NC_000023.9:g.38114415A>T | NCBI36 |
NG_008471.1:g.22736A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000039007.5:c.298+341A>T MANE Select | ENSP00000039007.4:n.298+341A>T | |
ENST00000643344.1:c.298+341A>T | ENSP00000496606.1:n.298+341A>T | |
ENST00000039007.4:c.298+341A>T | ENSP00000039007.4:n.298+341A>T | |
ENST00000465127.1:c.172-295903A>T | ENSP00000417050.1:n.172-295903A>T | |
ENST00000488812.1:n.353+378A>T | ||
NM_000531.5:c.298+341A>T | NP_000522.3:n.298+341A>T | |
XM_017029556.1:c.298+341A>T | XP_016885045.1:n.298+341A>T | |
NM_000531.6:c.298+341A>T MANE Select | NP_000522.3:n.298+341A>T |