HGVS | Genome Assembly |
---|---|
NC_000008.11:g.102208124A>G , CM000670.2:g.102208124A>G | GRCh38 |
NC_000008.10:g.103220352A>G , CM000670.1:g.103220352A>G | GRCh37 |
NC_000008.9:g.103289528A>G | NCBI36 |
NG_016617.1:g.35995T>C , LRG_788:g.35995T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000251810.8:c.*9T>C MANE Select | ENSP00000251810.3:n.*9T>C | |
ENST00000251810.7:c.*9T>C | ENSP00000251810.3:n.*9T>C | |
ENST00000395910.6:n.452T>C | ||
ENST00000522368.5:c.1234T>C | ||
ENST00000621845.1:c.*9T>C | ENSP00000484318.1:n.*9T>C | |
NM_001172477.1:c.*9T>C , LRG_788t1:c.*9T>C | NP_001165948.1:n.*9T>C | |
NM_001172478.1:c.*9T>C | NP_001165949.1:n.*9T>C | |
NM_015713.4:c.*9T>C , LRG_788t2:c.*9T>C | NP_056528.2:n.*9T>C | |
NM_001172478.2:c.*9T>C | NP_001165949.1:n.*9T>C | |
NM_015713.5:c.*9T>C MANE Select | NP_056528.2:n.*9T>C |