HGVS | Genome Assembly |
---|---|
NC_000010.11:g.119676627C= , CM000672.2:g.119676627C= | GRCh38 |
NC_000010.10:g.121436139C= , CM000672.1:g.121436139C= | GRCh37 |
NC_000010.9:g.121426129C= | NCBI36 |
NG_016125.1:g.30258C= , LRG_742:g.30258C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369085.8:c.1073C= MANE Select | ENSP00000358081.4:p.Pro358= | |
ENST00000369085.7:c.1073C= | ENSP00000358081.3:p.Pro358= | |
ENST00000450186.1:c.896C= | ENSP00000410036.1:p.Pro299= | |
NM_004281.3:c.1073C= , LRG_742t1:c.1073C= | NP_004272.2:p.Pro358= | |
XM_005270287.1:c.1070C= | XP_005270344.1:p.Pro357= | |
XM_005270287.2:c.1070C= | XP_005270344.1:p.Pro357= | |
NM_004281.4:c.1073C= MANE Select | NP_004272.2:p.Pro358= |