HGVS | Genome Assembly |
---|---|
NC_000023.11:g.136659138A>C , CM000685.2:g.136659138A>C | GRCh38 |
NC_000023.10:g.135741297A>C , CM000685.1:g.135741297A>C | GRCh37 |
NC_000023.9:g.135568963A>C | NCBI36 |
NG_007280.1:g.15962A>C , LRG_141:g.15962A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695724.1:c.*127A>C | ENSP00000512122.1:n.*127A>C | |
ENST00000695725.1:c.*64A>C | ENSP00000512123.1:n.*64A>C | |
ENST00000695726.1:n.2477A>C | ||
ENST00000695729.1:n.3312A>C | ||
ENST00000370629.7:c.509A>C MANE Select | ENSP00000359663.2:p.Tyr170Ser | |
ENST00000370628.2:c.446A>C | ENSP00000359662.2:p.Tyr149Ser | |
ENST00000370629.6:c.509A>C | ENSP00000359663.2:p.Tyr170Ser | |
NM_000074.2:c.509A>C , LRG_141t1:c.509A>C | NP_000065.1:p.Tyr170Ser | |
NM_000074.3:c.509A>C MANE Select | NP_000065.1:p.Tyr170Ser |