HGVS | Genome Assembly |
---|---|
NC_000014.9:g.102922753G= , CM000676.2:g.102922753G= | GRCh38 |
NC_000014.8:g.103389090G= , CM000676.1:g.103389090G= | GRCh37 |
NC_000014.7:g.102458843G= | NCBI36 |
NG_008276.2:g.5098G= , LRG_642:g.5098G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000299155.10:c.43+22G= MANE Select | ENSP00000299155.6:n.43+22G= | |
ENST00000299155.9:c.43+22G= | ENSP00000299155.5:n.43+22G= | |
NM_030943.3:c.43+22G= , LRG_642t1:c.43+22G= | NP_112205.2:n.43+22G= | |
XM_011537202.1:c.-120+3G= | XP_011535504.1:n.-120+3G= | |
XM_011537202.3:c.-120+3G= | XP_011535504.1:n.-120+3G= | |
XM_024449714.1:c.139+22G= | XP_024305482.1:n.139+22G= | |
NM_030943.4:c.43+22G= MANE Select | NP_112205.2:n.43+22G= |