HGVS | Genome Assembly |
---|---|
NC_000001.11:g.109264152C>T , CM000663.2:g.109264152C>T | GRCh38 |
NC_000001.10:g.109806774C>T , CM000663.1:g.109806774C>T | GRCh37 |
NC_000001.9:g.109608297C>T | NCBI36 |
NG_052669.1:g.19448C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271332.4:c.5076C>T MANE Select | ENSP00000271332.3:p.Gly1692= | |
ENST00000271332.3:c.5076C>T | ENSP00000271332.3:p.Gly1692= | |
NM_001408.2:c.5076C>T | NP_001399.1:p.Gly1692= | |
XM_005270580.3:c.5076C>T | XP_005270637.1:p.Gly1692= | |
NM_001408.3:c.5076C>T MANE Select | NP_001399.1:p.Gly1692= |