HGVS | Genome Assembly |
---|---|
NC_000002.12:g.202377397_202377405del , CM000664.2:g.202377397_202377405del | GRCh38 |
NC_000002.11:g.203242120_203242128del , CM000664.1:g.203242120_203242128del | GRCh37 |
NC_000002.10:g.202950365_202950373del | NCBI36 |
NG_009363.1:g.6071_6079del , LRG_712:g.6071_6079del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000374580.10:c.-78_-70del MANE Select | ENSP00000363708.4:n.-78_-70del | |
ENST00000374580.8:c.-78_-70del | ENSP00000363708.4:n.-78_-70del | |
NM_001204.6:c.-78_-70del , LRG_712t1:c.-78_-70del | NP_001195.2:n.-78_-70del | |
XM_011511687.1:c.-78_-70del | XP_011509989.1:n.-78_-70del | |
XM_011511688.1:c.-78_-70del | XP_011509990.1:n.-78_-70del | |
NM_001204.7:c.-78_-70del MANE Select | NP_001195.2:n.-78_-70del |