HGVS | Genome Assembly |
---|---|
NC_000007.14:g.19117354_19117355delinsCG , CM000669.2:g.19117354_19117355delinsCG | GRCh38 |
NC_000007.13:g.19156977_19156978delinsCG , CM000669.1:g.19156977_19156978delinsCG | GRCh37 |
NC_000007.12:g.19123502_19123503delinsCG | NCBI36 |
NG_008114.1:g.5318_5319delinsCG | |
NG_008114.2:g.5318_5319delinsCG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242261.6:c.-34_-33delinsCG MANE Select | ENSP00000242261.5:n.-34_-33delinsCG | |
ENST00000242261.5:c.-34_-33delinsCG | ENSP00000242261.5:n.-34_-33delinsCG | |
NM_000474.3:c.-34_-33delinsCG | NP_000465.1:n.-34_-33delinsCG | |
XM_011515496.1:c.-34_-33delinsCG | XP_011513798.1:n.-34_-33delinsCG | |
NR_149001.1:n.318_319delinsCG | ||
NM_000474.4:c.-34_-33delinsCG MANE Select | NP_000465.1:n.-34_-33delinsCG | |
NR_149001.2:n.282_283delinsCG |