HGVS | Genome Assembly |
---|---|
NC_000004.12:g.88007769_88007770delinsCG , CM000666.2:g.88007769_88007770delinsCG | GRCh38 |
NC_000004.11:g.88928921_88928922delinsCG , CM000666.1:g.88928921_88928922delinsCG | GRCh37 |
NC_000004.10:g.89147945_89147946delinsCG | NCBI36 |
NG_008604.1:g.5102_5103delinsCG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000237596.7:c.36_37delinsCG MANE Select | ENSP00000237596.2:p.Pro12= | |
ENST00000237596.6:c.36_37delinsCG | ENSP00000237596.2:p.Pro12= | |
NM_000297.3:c.36_37delinsCG | NP_000288.1:p.Pro12= | |
XM_011532028.1:c.36_37delinsCG | XP_011530330.1:p.Pro12= | |
XR_244632.2:n.131_132delinsCG | ||
NR_156488.1:n.123_124delinsCG | ||
XM_011532028.2:c.36_37delinsCG | XP_011530330.1:p.Pro12= | |
NM_000297.4:c.36_37delinsCG MANE Select | NP_000288.1:p.Pro12= | |
NR_156488.2:n.135_136delinsCG |