HGVS | Genome Assembly |
---|---|
NC_000006.12:g.49458130C>G , CM000668.2:g.49458130C>G | GRCh38 |
NC_000006.11:g.49425843C>G , CM000668.1:g.49425843C>G | GRCh37 |
NC_000006.10:g.49533802C>G | NCBI36 |
NG_007100.1:g.10010G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000274813.4:c.386-72G>C MANE Select | ENSP00000274813.3:n.386-72G>C | |
ENST00000274813.3:c.386-72G>C | ENSP00000274813.3:n.386-72G>C | |
NM_000255.3:c.386-72G>C | NP_000246.2:n.386-72G>C | |
XM_005249143.2:c.386-72G>C | XP_005249200.1:n.386-72G>C | |
XM_005249143.3:c.386-72G>C | XP_005249200.1:n.386-72G>C | |
NM_000255.4:c.386-72G>C MANE Select | NP_000246.2:n.386-72G>C |