HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23431496_23431497delinsGA , CM000676.2:g.23431496_23431497delinsGA | GRCh38 |
NC_000014.8:g.23900705_23900706delinsGA , CM000676.1:g.23900705_23900706delinsGA | GRCh37 |
NC_000014.7:g.22970545_22970546delinsGA | NCBI36 |
NG_007884.1:g.9165_9166delinsTC , LRG_384:g.9165_9166delinsTC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.733-16_733-15delinsTC MANE Select | ENSP00000347507.3:n.733-16_733-15delinsTC | |
ENST00000355349.3:c.733-16_733-15delinsTC | ENSP00000347507.3:n.733-16_733-15delinsTC | |
NM_000257.3:c.733-16_733-15delinsTC | NP_000248.2:n.733-16_733-15delinsTC | |
XR_245686.3:n.839-16_839-15delinsTC | ||
XM_017021340.1:c.733-16_733-15delinsTC | XP_016876829.1:n.733-16_733-15delinsTC | |
NM_000257.4:c.733-16_733-15delinsTC MANE Select | NP_000248.2:n.733-16_733-15delinsTC |