HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31524652A= , CM000680.2:g.31524652A= | GRCh38 |
NC_000018.9:g.29104615A= , CM000680.1:g.29104615A= | GRCh37 |
NC_000018.8:g.27358613A= | NCBI36 |
NG_007072.3:g.31411A= , LRG_397:g.31411A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682087.2:n.660-51A= | ||
ENST00000683614.2:n.660-51A= | ||
ENST00000682087.1:c.660-51A= | ||
ENST00000683614.1:c.660-51A= | ||
ENST00000261590.13:c.829-51A= MANE Select | ENSP00000261590.8:n.829-51A= | |
ENST00000261590.12:c.829-51A= | ENSP00000261590.8:n.829-51A= | |
NM_001943.3:c.829-51A= , LRG_397t1:c.829-51A= | NP_001934.2:n.829-51A= | |
NM_001943.4:c.829-51A= | NP_001934.2:n.829-51A= | |
XM_024451095.1:c.295-51A= | XP_024306863.1:n.295-51A= | |
NM_001943.5:c.829-51A= MANE Select | NP_001934.2:n.829-51A= |