HGVS | Genome Assembly |
---|---|
NC_000007.14:g.19117363_19117364insCGGCGGCCCG , CM000669.2:g.19117363_19117364insCGGCGGCCCG | GRCh38 |
NC_000007.13:g.19156986_19156987insCGGCGGCCCG , CM000669.1:g.19156986_19156987insCGGCGGCCCG | GRCh37 |
NC_000007.12:g.19123511_19123512insCGGCGGCCCG | NCBI36 |
NG_008114.1:g.5310_5311insGGGCCGCCGC | |
NG_008114.2:g.5310_5311insGGGCCGCCGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242261.6:c.-42_-41insGGGCCGCCGC MANE Select | ENSP00000242261.5:n.-42_-41insGGGCCGCCGC | |
ENST00000242261.5:c.-42_-41insGGGCCGCCGC | ENSP00000242261.5:n.-42_-41insGGGCCGCCGC | |
NM_000474.3:c.-42_-41insGGGCCGCCGC | NP_000465.1:n.-42_-41insGGGCCGCCGC | |
XM_011515496.1:c.-42_-41insGGGCCGCCGC | XP_011513798.1:n.-42_-41insGGGCCGCCGC | |
NR_149001.1:n.310_311insGGGCCGCCGC | ||
NM_000474.4:c.-42_-41insGGGCCGCCGC MANE Select | NP_000465.1:n.-42_-41insGGGCCGCCGC | |
NR_149001.2:n.274_275insGGGCCGCCGC |