HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32202685_32202686delinsGC , CM000668.2:g.32202685_32202686delinsGC | GRCh38 |
NC_000006.11:g.32170462_32170463delinsGC , CM000668.1:g.32170462_32170463delinsGC | GRCh37 |
NC_000006.10:g.32278440_32278441delinsGC | NCBI36 |
NG_028190.1:g.26382_26383delinsGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375023.3:c.3232-87_3232-86delinsGC MANE Select | ENSP00000364163.3:n.3232-87_3232-86delinsGC | |
ENST00000474612.1:n.1231_1232delinsGC | ||
NM_004557.3:c.3232-87_3232-86delinsGC | NP_004548.3:n.3232-87_3232-86delinsGC | |
NR_134949.1:n.3472+1084_3472+1085delinsGC | ||
NR_134950.1:n.3370+1084_3370+1085delinsGC | ||
NM_004557.4:c.3232-87_3232-86delinsGC MANE Select | NP_004548.3:n.3232-87_3232-86delinsGC | |
NR_134949.2:n.3472+1084_3472+1085delinsGC | ||
NR_134950.2:n.3370+1084_3370+1085delinsGC |