HGVS | Genome Assembly |
---|---|
NC_000010.11:g.87727323T>C , CM000672.2:g.87727323T>C | GRCh38 |
NC_000010.10:g.89487080T>C , CM000672.1:g.89487080T>C | GRCh37 |
NC_000010.9:g.89477060T>C | NCBI36 |
NG_012150.1:g.72605T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000456849.2:c.920T>C MANE Select | ENSP00000406157.1:p.Val307Ala | |
ENST00000361175.8:c.905T>C | ENSP00000354436.4:p.Val302Ala | |
ENST00000456849.1:c.920T>C | ENSP00000406157.1:p.Val307Ala | |
NM_001015880.1:c.920T>C | NP_001015880.1:p.Val307Ala | |
NM_004670.3:c.905T>C | NP_004661.2:p.Val302Ala | |
NM_001015880.2:c.920T>C MANE Select | NP_001015880.1:p.Val307Ala | |
NM_004670.4:c.905T>C | NP_004661.2:p.Val302Ala |