HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154954037C>A , CM000685.2:g.154954037C>A | GRCh38 |
NC_000023.10:g.154182312C>A , CM000685.1:g.154182312C>A | GRCh37 |
NC_000023.9:g.153835506C>A | NCBI36 |
NG_011403.1:g.73687G>T | |
NG_011403.2:g.73687G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.1758G>T MANE Select | ENSP00000353393.4:p.Met586Ile | |
ENST00000647125.1:c.*1634G>T | ENSP00000496062.1:n.*1634G>T | |
ENST00000360256.8:c.1758G>T | ENSP00000353393.4:p.Met586Ile | |
NM_000132.3:c.1758G>T | NP_000123.1:p.Met586Ile | |
XM_011531126.1:c.1653G>T | XP_011529428.1:p.Met551Ile | |
NM_000132.4:c.1758G>T MANE Select | NP_000123.1:p.Met586Ile |