HGVS | Genome Assembly |
---|---|
NC_000010.11:g.114044261G>C , CM000672.2:g.114044261G>C | GRCh38 |
NC_000010.10:g.115804020G>C , CM000672.1:g.115804020G>C | GRCh37 |
NC_000010.9:g.115794010G>C | NCBI36 |
NG_012187.1:g.5215G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369295.4:c.129G>C MANE Select | ENSP00000358301.2:p.Leu43= | |
ENST00000369295.3:c.129G>C | ENSP00000358301.2:p.Leu43= | |
NM_000684.2:c.129G>C | NP_000675.1:p.Leu43= | |
NM_000684.3:c.129G>C MANE Select | NP_000675.1:p.Leu43= |