HGVS | Genome Assembly |
---|---|
NC_000001.11:g.215781789A>G , CM000663.2:g.215781789A>G | GRCh38 |
NC_000001.10:g.215955131A>G , CM000663.1:g.215955131A>G | GRCh37 |
NC_000001.9:g.214021754A>G | NCBI36 |
NG_009497.1:g.646608T>C | |
NG_009497.2:g.646660T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.10740+253T>C MANE Select | ENSP00000305941.3:n.10740+253T>C | |
ENST00000674083.1:c.10740+253T>C | ENSP00000501296.1:n.10740+253T>C | |
ENST00000307340.7:c.10740+253T>C | ENSP00000305941.3:n.10740+253T>C | |
NM_206933.2:c.10740+253T>C | NP_996816.2:n.10740+253T>C | |
NM_206933.3:c.10740+253T>C | NP_996816.2:n.10740+253T>C | |
NM_206933.4:c.10740+253T>C MANE Select | NP_996816.3:n.10740+253T>C |