HGVS | Genome Assembly |
---|---|
NC_000024.10:g.20579786T>C , CM000686.2:g.20579786T>C | GRCh38 |
NC_000024.9:g.22741672T>C , CM000686.1:g.22741672T>C | GRCh37 |
NC_000024.8:g.21151060T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361365.7:c.100+95T>C MANE Select | ENSP00000354722.2:n.100+95T>C | |
ENST00000361365.6:c.100+95T>C | ENSP00000354722.2:n.100+95T>C | |
ENST00000382772.3:c.100+95T>C | ENSP00000372222.3:n.100+95T>C | |
ENST00000465253.1:n.194+95T>C | ||
NM_001278612.1:c.100+95T>C | NP_001265541.1:n.100+95T>C | |
NM_004681.3:c.100+95T>C | NP_004672.2:n.100+95T>C | |
NM_004681.4:c.100+95T>C MANE Select | NP_004672.2:n.100+95T>C | |
NM_001278612.2:c.100+95T>C | NP_001265541.1:n.100+95T>C |