HGVS | Genome Assembly |
---|---|
NC_000011.10:g.65868603A>G , CM000673.2:g.65868603A>G | GRCh38 |
NC_000011.9:g.65636074A>G , CM000673.1:g.65636074A>G | GRCh37 |
NC_000011.8:g.65392650A>G | NCBI36 |
NG_012304.2:g.9332T>C | |
NG_053116.1:g.13542A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307998.11:c.754T>C MANE Select | ENSP00000309953.6:p.Tyr252His | |
ENST00000307998.10:c.754T>C | ENSP00000309953.6:p.Tyr252His | |
ENST00000526628.5:n.1320T>C | ||
ENST00000527969.1:n.1439T>C | ||
ENST00000528176.5:c.754T>C | ENSP00000434151.1:p.Tyr252His | |
ENST00000531005.5:n.1748T>C | ||
ENST00000531972.5:c.754T>C | ENSP00000435295.1:p.Tyr252His | |
ENST00000532084.5:n.180T>C | ||
NM_016938.4:c.754T>C | NP_058634.4:p.Tyr252His | |
NR_037718.1:n.1013T>C | ||
NM_016938.5:c.754T>C MANE Select | NP_058634.4:p.Tyr252His | |
NR_037718.2:n.879T>C |