HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23434031_23434032delinsAC , CM000676.2:g.23434031_23434032delinsAC | GRCh38 |
NC_000014.8:g.23903240_23903241delinsAC , CM000676.1:g.23903240_23903241delinsAC | GRCh37 |
NC_000014.7:g.22973080_22973081delinsAC | NCBI36 |
NG_007884.1:g.6630_6631delinsGT , LRG_384:g.6630_6631delinsGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.-9+162_-9+163delinsGT MANE Select | ENSP00000347507.3:n.-9+162_-9+163delinsGT | |
ENST00000355349.3:c.-9+162_-9+163delinsGT | ENSP00000347507.3:n.-9+162_-9+163delinsGT | |
NM_000257.3:c.-9+162_-9+163delinsGT | NP_000248.2:n.-9+162_-9+163delinsGT | |
XR_245686.3:n.98+162_98+163delinsGT | ||
XM_017021340.1:c.-8-292_-8-291delinsGT | XP_016876829.1:n.-8-292_-8-291delinsGT | |
NM_000257.4:c.-9+162_-9+163delinsGT MANE Select | NP_000248.2:n.-9+162_-9+163delinsGT |