HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41624224C>A , CM000679.2:g.41624224C>A | GRCh38 |
NC_000017.10:g.39780476C>A , CM000679.1:g.39780476C>A | GRCh37 |
NC_000017.9:g.37034002C>A | NCBI36 |
NG_008625.1:g.5407G>T | |
NG_009090.2:g.167489G>T , LRG_401:g.167489G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000311208.13:c.286G>T MANE Select | ENSP00000308452.8:p.Ala96Ser | |
ENST00000311208.12:c.286G>T | ENSP00000308452.8:p.Ala96Ser | |
ENST00000463128.5:c.-312-18G>T | ENSP00000468672.1:n.-312-18G>T | |
ENST00000491673.1:n.352G>T | ||
ENST00000493253.5:n.73G>T | ||
ENST00000540235.5:c.71+10G>T | ENSP00000441751.2:n.71+10G>T | |
ENST00000577817.3:c.241G>T | ENSP00000467418.1:p.Ala81Ser | |
NM_000422.2:c.286G>T | NP_000413.1:p.Ala96Ser | |
NM_000422.3:c.286G>T MANE Select | NP_000413.1:p.Ala96Ser |