HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240878918_240878919delinsTG , CM000664.2:g.240878918_240878919delinsTG | GRCh38 |
NC_000002.11:g.241818335_241818336delinsTG , CM000664.1:g.241818335_241818336delinsTG | GRCh37 |
NC_000002.10:g.241467008_241467009delinsTG | NCBI36 |
NG_008005.1:g.15174_15175delinsTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307503.4:c.*97_*98delinsTG MANE Select | ENSP00000302620.3:n.*97_*98delinsTG | |
ENST00000307503.3:c.*97_*98delinsTG | ENSP00000302620.3:n.*97_*98delinsTG | |
ENST00000470255.1:n.1054_1055delinsTG | ||
NM_000030.2:c.*97_*98delinsTG | NP_000021.1:n.*97_*98delinsTG | |
NM_000030.3:c.*97_*98delinsTG MANE Select | NP_000021.1:n.*97_*98delinsTG |