HGVS | Genome Assembly |
---|---|
NC_000019.10:g.33521820A>G , CM000681.2:g.33521820A>G | GRCh38 |
NC_000019.9:g.34012726A>G , CM000681.1:g.34012726A>G | GRCh37 |
NC_000019.8:g.38704566A>G | NCBI36 |
NG_013358.1:g.5074T>C | |
NG_013358.2:g.5074T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698361.1:c.-60T>C | ENSP00000513684.1:n.-60T>C | |
ENST00000698362.1:c.-60T>C | ENSP00000513685.1:n.-60T>C | |
ENST00000698363.1:n.4T>C | ||
ENST00000698364.1:n.4T>C | ||
ENST00000698365.1:n.4T>C | ||
NM_000285.3:c.-60T>C | NP_000276.2:n.-60T>C | |
NM_001166056.1:c.-60T>C | NP_001159528.1:n.-60T>C | |
NM_001166057.1:c.-60T>C | NP_001159529.1:n.-60T>C |