HGVS | Genome Assembly |
---|---|
NC_000005.10:g.14871551_14871552insGC , CM000667.2:g.14871551_14871552insGC | GRCh38 |
NC_000005.9:g.14871660_14871661insGC , CM000667.1:g.14871660_14871661insGC | GRCh37 |
NC_000005.8:g.14924660_14924661insGC | NCBI36 |
NG_008273.1:g.5228_5229insCG | |
NG_008273.2:g.5235_5236insCG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000284268.8:c.-104_-103insCG MANE Select | ENSP00000284268.6:n.-104_-103insCG | |
ENST00000284268.6:c.-104_-103insCG | ENSP00000284268.6:n.-104_-103insCG | |
ENST00000505140.1:c.-104_-103insCG | ENSP00000426332.1:n.-104_-103insCG | |
NM_054027.4:c.-104_-103insCG | NP_473368.1:n.-104_-103insCG | |
XM_011514067.1:c.-104_-103insCG | XP_011512369.1:n.-104_-103insCG | |
NM_054027.5:c.-104_-103insCG | NP_473368.1:n.-104_-103insCG | |
NM_054027.6:c.-104_-103insCG MANE Select | NP_473368.1:n.-104_-103insCG |