HGVS | Genome Assembly |
---|---|
NC_000014.9:g.28767782G>C , CM000676.2:g.28767782G>C | GRCh38 |
NC_000014.8:g.29236988G>C , CM000676.1:g.29236988G>C | GRCh37 |
NC_000014.7:g.28306739G>C | NCBI36 |
NG_009367.1:g.5702G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706482.1:c.503G>C | ENSP00000516406.1:p.Gly168Ala | |
ENST00000313071.7:c.503G>C MANE Select | ENSP00000339004.3:p.Gly168Ala | |
ENST00000313071.6:c.503G>C | ENSP00000339004.3:p.Gly168Ala | |
NM_005249.4:c.503G>C | NP_005240.3:p.Gly168Ala | |
NM_005249.5:c.503G>C MANE Select | NP_005240.3:p.Gly168Ala |