HGVS | Genome Assembly |
---|---|
NC_000010.11:g.119670152A>C , CM000672.2:g.119670152A>C | GRCh38 |
NC_000010.10:g.121429664A>C , CM000672.1:g.121429664A>C | GRCh37 |
NC_000010.9:g.121419654A>C | NCBI36 |
NG_016125.1:g.23783A>C , LRG_742:g.23783A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369085.8:c.482A>C MANE Select | ENSP00000358081.4:p.Gln161Pro | |
ENST00000369085.7:c.482A>C | ENSP00000358081.3:p.Gln161Pro | |
ENST00000450186.1:c.308A>C | ENSP00000410036.1:p.Gln103Pro | |
NM_004281.3:c.482A>C , LRG_742t1:c.482A>C | NP_004272.2:p.Gln161Pro | |
XM_005270287.1:c.482A>C | XP_005270344.1:p.Gln161Pro | |
XM_005270287.2:c.482A>C | XP_005270344.1:p.Gln161Pro | |
NM_004281.4:c.482A>C MANE Select | NP_004272.2:p.Gln161Pro |