HGVS | Genome Assembly |
---|---|
NC_000011.10:g.116835800C= , CM000673.2:g.116835800C= | GRCh38 |
NC_000011.9:g.116706516C= , CM000673.1:g.116706516C= | GRCh37 |
NC_000011.8:g.116211726C= | NCBI36 |
NG_012021.1:g.6823G= , LRG_767:g.6823G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000236850.5:c.*8G= MANE Select | ENSP00000236850.3:n.*8G= | |
ENST00000236850.4:c.*8G= | ENSP00000236850.3:n.*8G= | |
ENST00000359492.6:c.*8G= | ENSP00000352471.2:n.*8G= | |
ENST00000375320.5:c.*8G= | ENSP00000364469.1:n.*8G= | |
ENST00000375323.5:c.*8G= | ENSP00000364472.1:n.*8G= | |
ENST00000375329.6:c.*8G= | ENSP00000364478.2:n.*8G= | |
NM_000039.1:c.*8G= , LRG_767t1:c.*8G= | NP_000030.1:n.*8G= | |
XM_005271539.2:c.*8G= | XP_005271596.1:n.*8G= | |
XM_005271540.1:c.*8G= | XP_005271597.1:n.*8G= | |
NM_000039.2:c.*8G= | NP_000030.1:n.*8G= | |
NM_001318017.1:c.*8G= | NP_001304946.1:n.*8G= | |
NM_001318018.1:c.*8G= | NP_001304947.1:n.*8G= | |
NM_001318021.1:c.*8G= | NP_001304950.1:n.*8G= | |
NM_001318017.2:c.*8G= | NP_001304946.1:n.*8G= | |
NM_001318018.2:c.*8G= | NP_001304947.1:n.*8G= | |
NM_000039.3:c.*8G= MANE Select | NP_000030.1:n.*8G= |