HGVS | Genome Assembly |
---|---|
NC_000011.10:g.65868585A>T , CM000673.2:g.65868585A>T | GRCh38 |
NC_000011.9:g.65636056A>T , CM000673.1:g.65636056A>T | GRCh37 |
NC_000011.8:g.65392632A>T | NCBI36 |
NG_012304.2:g.9350T>A | |
NG_053116.1:g.13524A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307998.11:c.772T>A MANE Select | ENSP00000309953.6:p.Cys258Ser | |
ENST00000307998.10:c.772T>A | ENSP00000309953.6:p.Cys258Ser | |
ENST00000526628.5:n.1338T>A | ||
ENST00000527969.1:n.1457T>A | ||
ENST00000528176.5:c.772T>A | ENSP00000434151.1:p.Cys258Ser | |
ENST00000531005.5:n.1766T>A | ||
ENST00000531972.5:c.772T>A | ENSP00000435295.1:p.Cys258Ser | |
ENST00000532084.5:n.198T>A | ||
NM_016938.4:c.772T>A | NP_058634.4:p.Cys258Ser | |
NR_037718.1:n.1031T>A | ||
NM_016938.5:c.772T>A MANE Select | NP_058634.4:p.Cys258Ser | |
NR_037718.2:n.897T>A |