HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94781856C>T , CM000672.2:g.94781856C>T | GRCh38 |
NC_000010.10:g.96541613C>T , CM000672.1:g.96541613C>T | GRCh37 |
NC_000010.9:g.96531603C>T | NCBI36 |
NG_008384.2:g.24151C>T | |
NG_008384.3:g.24176C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.678C>T MANE Select | ENSP00000360372.3:p.Phe226= | |
ENST00000645461.1:n.1731C>T | ||
ENST00000371321.7:c.678C>T | ENSP00000360372.3:p.Phe226= | |
ENST00000464755.1:c.1441C>T | ENSP00000483243.1:n.1441C>T | |
NM_000769.2:c.678C>T | NP_000760.1:p.Phe226= | |
NM_000769.4:c.678C>T MANE Select | NP_000760.1:p.Phe226= |