HGVS | Genome Assembly |
---|---|
NC_000007.14:g.19117416_19117417insT , CM000669.2:g.19117416_19117417insT | GRCh38 |
NC_000007.13:g.19157039_19157040insT , CM000669.1:g.19157039_19157040insT | GRCh37 |
NC_000007.12:g.19123564_19123565insT | NCBI36 |
NG_008114.1:g.5256_5257insA | |
NG_008114.2:g.5256_5257insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242261.6:c.-96_-95insA MANE Select | ENSP00000242261.5:n.-96_-95insA | |
ENST00000242261.5:c.-96_-95insA | ENSP00000242261.5:n.-96_-95insA | |
NM_000474.3:c.-96_-95insA | NP_000465.1:n.-96_-95insA | |
XM_011515496.1:c.-96_-95insA | XP_011513798.1:n.-96_-95insA | |
NR_149001.1:n.256_257insA | ||
NM_000474.4:c.-96_-95insA MANE Select | NP_000465.1:n.-96_-95insA | |
NR_149001.2:n.220_221insA |