HGVS | Genome Assembly |
---|---|
NC_000010.11:g.104038340C>A , CM000672.2:g.104038340C>A | GRCh38 |
NC_000010.10:g.105798098C>A , CM000672.1:g.105798098C>A | GRCh37 |
NC_000010.9:g.105788088C>A | NCBI36 |
NG_007069.1:g.52541G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369733.8:c.2935+66G>T | ENSP00000358748.3:n.2935+66G>T | |
ENST00000648076.2:c.3070+66G>T MANE Select | ENSP00000497653.1:n.3070+66G>T | |
ENST00000353479.9:c.3070+66G>T | ENSP00000340937.5:n.3070+66G>T | |
ENST00000369733.7:c.2935+66G>T | ENSP00000358748.3:n.2935+66G>T | |
NM_000494.3:c.3070+66G>T | NP_000485.3:n.3070+66G>T | |
NM_000494.4:c.3070+66G>T MANE Select | NP_000485.3:n.3070+66G>T |