HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48474280G>C , CM000677.2:g.48474280G>C | GRCh38 |
NC_000015.9:g.48766477G>C , CM000677.1:g.48766477G>C | GRCh37 |
NC_000015.8:g.46553769G>C | NCBI36 |
NG_008805.2:g.176509C>G , LRG_778:g.176509C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.4185C>G | ENSP00000453958.2:p.Tyr1395Ter | |
ENST00000674301.2:c.4185C>G | ENSP00000501333.2:p.Tyr1395Ter | |
ENST00000684448.1:n.2859C>G | ||
ENST00000316623.10:c.4185C>G MANE Select | ENSP00000325527.5:p.Tyr1395Ter | |
ENST00000316623.9:c.4185C>G | ENSP00000325527.5:p.Tyr1395Ter | |
ENST00000537463.6:c.857C>G | ENSP00000440294.2:p.Thr286Arg | |
NM_000138.4:c.4185C>G , LRG_778t1:c.4185C>G | NP_000129.3:p.Tyr1395Ter | |
NM_000138.5:c.4185C>G MANE Select | NP_000129.3:p.Tyr1395Ter |