HGVS | Genome Assembly |
---|---|
NC_000019.10:g.35845977_35845978delinsGC , CM000681.2:g.35845977_35845978delinsGC | GRCh38 |
NC_000019.9:g.36336879_36336880delinsGC , CM000681.1:g.36336879_36336880delinsGC | GRCh37 |
NC_000019.8:g.41028719_41028720delinsGC | NCBI36 |
NG_013356.2:g.28310_28311delinsGC , LRG_693:g.28310_28311delinsGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378910.10:c.1627+30_1627+31delinsGC MANE Select | ENSP00000368190.4:n.1627+30_1627+31delinsGC | |
ENST00000353632.6:c.1627+30_1627+31delinsGC | ENSP00000343634.5:n.1627+30_1627+31delinsGC | |
ENST00000378910.9:c.1627+30_1627+31delinsGC | ENSP00000368190.4:n.1627+30_1627+31delinsGC | |
NM_004646.3:c.1627+30_1627+31delinsGC , LRG_693t1:c.1627+30_1627+31delinsGC | NP_004637.1:n.1627+30_1627+31delinsGC | |
NM_004646.4:c.1627+30_1627+31delinsGC MANE Select | NP_004637.1:n.1627+30_1627+31delinsGC |