HGVS | Genome Assembly |
---|---|
NC_000011.10:g.65868573G>T , CM000673.2:g.65868573G>T | GRCh38 |
NC_000011.9:g.65636044G>T , CM000673.1:g.65636044G>T | GRCh37 |
NC_000011.8:g.65392620G>T | NCBI36 |
NG_012304.2:g.9362C>A | |
NG_053116.1:g.13512G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307998.11:c.784C>A MANE Select | ENSP00000309953.6:p.Pro262Thr | |
ENST00000307998.10:c.784C>A | ENSP00000309953.6:p.Pro262Thr | |
ENST00000526628.5:n.1350C>A | ||
ENST00000527969.1:n.1469C>A | ||
ENST00000528176.5:c.784C>A | ENSP00000434151.1:p.Pro262Thr | |
ENST00000531005.5:n.1778C>A | ||
ENST00000531972.5:c.784C>A | ENSP00000435295.1:p.Pro262Thr | |
ENST00000532084.5:n.210C>A | ||
NM_016938.4:c.784C>A | NP_058634.4:p.Pro262Thr | |
NR_037718.1:n.1043C>A | ||
NM_016938.5:c.784C>A MANE Select | NP_058634.4:p.Pro262Thr | |
NR_037718.2:n.909C>A |