HGVS | Genome Assembly |
---|---|
NC_000014.9:g.91272474T>C , CM000676.2:g.91272474T>C | GRCh38 |
NC_000014.8:g.91738818T>C , CM000676.1:g.91738818T>C | GRCh37 |
NC_000014.7:g.90808571T>C | NCBI36 |
NG_033118.1:g.150371A>G | |
NG_033118.2:g.150371A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000389857.11:c.*151A>G MANE Select | ENSP00000374507.6:n.*151A>G | |
ENST00000331194.8:c.*151A>G | ENSP00000330332.8:n.*151A>G | |
ENST00000389857.10:c.*151A>G | ENSP00000374507.6:n.*151A>G | |
ENST00000556726.5:c.2466A>G | ||
NM_001080414.3:c.*151A>G | NP_001073883.2:n.*151A>G | |
XM_011536796.1:c.*151A>G | XP_011535098.1:n.*151A>G | |
XM_011536796.2:c.*151A>G | XP_011535098.1:n.*151A>G | |
XM_017021336.1:c.*151A>G | XP_016876825.1:n.*151A>G | |
NM_001080414.4:c.*151A>G MANE Select | NP_001073883.2:n.*151A>G |