HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23420374_23420375insCTG , CM000676.2:g.23420374_23420375insCTG | GRCh38 |
NC_000014.8:g.23889583_23889584insCTG , CM000676.1:g.23889583_23889584insCTG | GRCh37 |
NC_000014.7:g.22959423_22959424insCTG | NCBI36 |
NG_007884.1:g.20288_20289insAGC , LRG_384:g.20288_20289insAGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.3337-140_3337-139insAGC MANE Select | ENSP00000347507.3:n.3337-140_3337-139insAGC | |
ENST00000355349.3:c.3337-140_3337-139insAGC | ENSP00000347507.3:n.3337-140_3337-139insAGC | |
NM_000257.3:c.3337-140_3337-139insAGC | NP_000248.2:n.3337-140_3337-139insAGC | |
XR_245686.3:n.3445-140_3445-139insAGC | ||
XM_017021340.1:c.3337-140_3337-139insAGC | XP_016876829.1:n.3337-140_3337-139insAGC | |
NM_000257.4:c.3337-140_3337-139insAGC MANE Select | NP_000248.2:n.3337-140_3337-139insAGC |