HGVS | Genome Assembly |
---|---|
NC_000013.11:g.110169617T= , CM000675.2:g.110169617T= | GRCh38 |
NC_000013.10:g.110821964T= , CM000675.1:g.110821964T= | GRCh37 |
NC_000013.9:g.109619965T= | NCBI36 |
NG_011544.2:g.142533A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000375820.10:c.3876+12A= MANE Select | ENSP00000364979.4:n.3876+12A= | |
ENST00000650424.1:c.32+12A= | ||
ENST00000375820.8:c.3876+12A= | ENSP00000364979.4:n.3876+12A= | |
NM_001845.5:c.3876+12A= | NP_001836.3:n.3876+12A= | |
XM_011521048.1:c.3684+12A= | XP_011519350.1:n.3684+12A= | |
XM_011521048.2:c.3684+12A= | XP_011519350.1:n.3684+12A= | |
NM_001845.6:c.3876+12A= MANE Select | NP_001836.3:n.3876+12A= |