HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154901951T>A , CM000685.2:g.154901951T>A | GRCh38 |
NC_000023.10:g.154130226T>A , CM000685.1:g.154130226T>A | GRCh37 |
NC_000023.9:g.153783420T>A | NCBI36 |
NG_011403.1:g.125773A>T | |
NG_011403.2:g.125773A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.6115+100A>T MANE Select | ENSP00000353393.4:n.6115+100A>T | |
ENST00000360256.8:c.6115+100A>T | ENSP00000353393.4:n.6115+100A>T | |
NM_000132.3:c.6115+100A>T | NP_000123.1:n.6115+100A>T | |
XM_011531126.1:c.6010+100A>T | XP_011529428.1:n.6010+100A>T | |
NM_000132.4:c.6115+100A>T MANE Select | NP_000123.1:n.6115+100A>T |