HGVS | Genome Assembly |
---|---|
NC_000023.11:g.137567319T>G , CM000685.2:g.137567319T>G | GRCh38 |
NC_000023.10:g.136649478T>G , CM000685.1:g.136649478T>G | GRCh37 |
NC_000023.9:g.136477144T>G | NCBI36 |
NG_008115.1:g.6133T>G | |
NG_008115.2:g.6193T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000287538.10:c.628T>G MANE Select | ENSP00000287538.5:p.Tyr210Asp | |
ENST00000287538.9:c.628T>G | ENSP00000287538.5:p.Tyr210Asp | |
ENST00000370606.3:c.628T>G | ENSP00000359638.3:p.Tyr210Asp | |
NM_003413.3:c.628T>G | NP_003404.1:p.Tyr210Asp | |
NM_001330661.1:c.628T>G | NP_001317590.1:p.Tyr210Asp | |
NM_003413.4:c.628T>G MANE Select | NP_003404.1:p.Tyr210Asp |