HGVS | Genome Assembly |
---|---|
NC_000009.12:g.4507192G>C , CM000671.2:g.4507192G>C | GRCh38 |
NC_000009.11:g.4507192G>C , CM000671.1:g.4507192G>C | GRCh37 |
NC_000009.10:g.4497192G>C | NCBI36 |
NG_017044.1:g.21766G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262352.8:c.91+16422G>C MANE Select | ENSP00000262352.3:n.91+16422G>C | |
ENST00000262352.7:c.91+16422G>C | ENSP00000262352.3:n.91+16422G>C | |
NM_004170.5:c.91+16422G>C | NP_004161.4:n.91+16422G>C | |
XM_011518007.1:c.92-12636G>C | XP_011516309.1:n.92-12636G>C | |
XM_011518010.1:c.91+16422G>C | XP_011516312.1:n.91+16422G>C | |
XM_017015042.1:c.92-12636G>C | XP_016870531.1:n.92-12636G>C | |
XM_017015043.1:c.91+16422G>C | XP_016870532.1:n.91+16422G>C | |
NM_004170.6:c.91+16422G>C MANE Select | NP_004161.4:n.91+16422G>C |