HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23421169_23421170delinsTG , CM000676.2:g.23421169_23421170delinsTG | GRCh38 |
NC_000014.8:g.23890378_23890379delinsTG , CM000676.1:g.23890378_23890379delinsTG | GRCh37 |
NC_000014.7:g.22960218_22960219delinsTG | NCBI36 |
NG_007884.1:g.19492_19493delinsCA , LRG_384:g.19492_19493delinsCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.3246-122_3246-121delinsCA MANE Select | ENSP00000347507.3:n.3246-122_3246-121delinsCA | |
ENST00000355349.3:c.3246-122_3246-121delinsCA | ENSP00000347507.3:n.3246-122_3246-121delinsCA | |
NM_000257.3:c.3246-122_3246-121delinsCA | NP_000248.2:n.3246-122_3246-121delinsCA | |
XR_245686.3:n.3354-122_3354-121delinsCA | ||
XM_017021340.1:c.3246-122_3246-121delinsCA | XP_016876829.1:n.3246-122_3246-121delinsCA | |
NM_000257.4:c.3246-122_3246-121delinsCA MANE Select | NP_000248.2:n.3246-122_3246-121delinsCA |