HGVS | Genome Assembly |
---|---|
NC_000006.12:g.3225880A>G , CM000668.2:g.3225880A>G | GRCh38 |
NC_000006.11:g.3226114A>G , CM000668.1:g.3226114A>G | GRCh37 |
NC_000006.10:g.3171113A>G | NCBI36 |
NG_016715.1:g.6855T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259818.8:c.278-69T>C MANE Select | ENSP00000259818.6:n.278-69T>C | |
ENST00000680070.1:n.1208-69T>C | ||
ENST00000681707.1:n.1105-69T>C | ||
ENST00000681757.1:n.583-69T>C | ||
ENST00000259818.7:c.278-69T>C | ENSP00000259818.6:n.278-69T>C | |
ENST00000473006.1:n.395-69T>C | ||
NM_178012.4:c.278-69T>C | NP_821080.1:n.278-69T>C | |
XM_011514571.1:c.62-69T>C | XP_011512873.1:n.62-69T>C | |
NM_178012.5:c.278-69T>C MANE Select | NP_821080.1:n.278-69T>C |