HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23423404_23423405delinsTC , CM000676.2:g.23423404_23423405delinsTC | GRCh38 |
NC_000014.8:g.23892613_23892614delinsTC , CM000676.1:g.23892613_23892614delinsTC | GRCh37 |
NC_000014.7:g.22962453_22962454delinsTC | NCBI36 |
NG_007884.1:g.17257_17258delinsGA , LRG_384:g.17257_17258delinsGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.3099+142_3099+143delinsGA MANE Select | ENSP00000347507.3:n.3099+142_3099+143delinsGA | |
ENST00000355349.3:c.3099+142_3099+143delinsGA | ENSP00000347507.3:n.3099+142_3099+143delinsGA | |
NM_000257.3:c.3099+142_3099+143delinsGA | NP_000248.2:n.3099+142_3099+143delinsGA | |
XR_245686.3:n.3205+142_3205+143delinsGA | ||
XM_017021340.1:c.3099+142_3099+143delinsGA | XP_016876829.1:n.3099+142_3099+143delinsGA | |
NM_000257.4:c.3099+142_3099+143delinsGA MANE Select | NP_000248.2:n.3099+142_3099+143delinsGA |