HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48489971A>C , CM000677.2:g.48489971A>C | GRCh38 |
NC_000015.9:g.48782168A>C , CM000677.1:g.48782168A>C | GRCh37 |
NC_000015.8:g.46569460A>C | NCBI36 |
NG_008805.2:g.160818T>G , LRG_778:g.160818T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.2962T>G | ENSP00000453958.2:p.Trp988Gly | |
ENST00000674301.2:c.2962T>G | ENSP00000501333.2:p.Trp988Gly | |
ENST00000684448.1:n.1636T>G | ||
ENST00000316623.10:c.2962T>G MANE Select | ENSP00000325527.5:p.Trp988Gly | |
ENST00000316623.9:c.2962T>G | ENSP00000325527.5:p.Trp988Gly | |
ENST00000537463.6:c.637-15321T>G | ENSP00000440294.2:n.637-15321T>G | |
NM_000138.4:c.2962T>G , LRG_778t1:c.2962T>G | NP_000129.3:p.Trp988Gly | |
NM_000138.5:c.2962T>G MANE Select | NP_000129.3:p.Trp988Gly |