HGVS | Genome Assembly |
---|---|
NC_000012.12:g.69350126G>C , CM000674.2:g.69350126G>C | GRCh38 |
NC_000012.11:g.69743906G>C , CM000674.1:g.69743906G>C | GRCh37 |
NC_000012.10:g.68030173G>C | NCBI36 |
NG_008195.1:g.6773G>C , LRG_768:g.6773G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261267.7:c.155G>C MANE Select | ENSP00000261267.2:p.Trp52Ser | |
ENST00000261267.6:c.155G>C | ENSP00000261267.2:p.Trp52Ser | |
ENST00000548839.1:c.155G>C | ENSP00000449969.1:p.Trp52Ser | |
ENST00000549690.1:c.155G>C | ENSP00000449898.1:p.Trp52Ser | |
NM_000239.2:c.155G>C , LRG_768t1:c.155G>C | NP_000230.1:p.Trp52Ser | |
NM_000239.3:c.155G>C MANE Select | NP_000230.1:p.Trp52Ser |