HGVS | Genome Assembly |
---|---|
NC_000010.11:g.119651653C= , CM000672.2:g.119651653C= | GRCh38 |
NC_000010.10:g.121411165C= , CM000672.1:g.121411165C= | GRCh37 |
NC_000010.9:g.121401155C= | NCBI36 |
NG_016125.1:g.5284C= , LRG_742:g.5284C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369085.8:c.-23C= MANE Select | ENSP00000358081.4:n.-23C= | |
ENST00000369085.7:c.-23C= | ENSP00000358081.3:n.-23C= | |
NM_004281.3:c.-23C= , LRG_742t1:c.-23C= | NP_004272.2:n.-23C= | |
XM_005270287.1:c.-23C= | XP_005270344.1:n.-23C= | |
XM_005270287.2:c.-23C= | XP_005270344.1:n.-23C= | |
NM_004281.4:c.-23C= MANE Select | NP_004272.2:n.-23C= |