HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23420855_23420856delinsAT , CM000676.2:g.23420855_23420856delinsAT | GRCh38 |
NC_000014.8:g.23890064_23890065delinsAT , CM000676.1:g.23890064_23890065delinsAT | GRCh37 |
NC_000014.7:g.22959904_22959905delinsAT | NCBI36 |
NG_007884.1:g.19806_19807delinsAT , LRG_384:g.19806_19807delinsAT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.3336+102_3336+103delinsAT MANE Select | ENSP00000347507.3:n.3336+102_3336+103delinsAT | |
ENST00000355349.3:c.3336+102_3336+103delinsAT | ENSP00000347507.3:n.3336+102_3336+103delinsAT | |
NM_000257.3:c.3336+102_3336+103delinsAT | NP_000248.2:n.3336+102_3336+103delinsAT | |
XR_245686.3:n.3444+102_3444+103delinsAT | ||
XM_017021340.1:c.3336+102_3336+103delinsAT | XP_016876829.1:n.3336+102_3336+103delinsAT | |
NM_000257.4:c.3336+102_3336+103delinsAT MANE Select | NP_000248.2:n.3336+102_3336+103delinsAT |