HGVS | Genome Assembly |
---|---|
NC_000022.11:g.43929163T>C , CM000684.2:g.43929163T>C | GRCh38 |
NC_000022.10:g.44325043T>C , CM000684.1:g.44325043T>C | GRCh37 |
NC_000022.9:g.42656376T>C | NCBI36 |
NG_008631.1:g.10425T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000216180.8:c.486+274T>C MANE Select | ENSP00000216180.3:n.486+274T>C | |
ENST00000216180.7:c.486+274T>C | ENSP00000216180.3:n.486+274T>C | |
ENST00000406117.6:c.*118+274T>C | ENSP00000384668.2:n.*118+274T>C | |
ENST00000423180.2:c.474+274T>C | ENSP00000397987.2:n.474+274T>C | |
ENST00000478713.1:n.520+274T>C | ||
NM_025225.2:c.486+274T>C | NP_079501.2:n.486+274T>C | |
NM_025225.3:c.486+274T>C MANE Select | NP_079501.2:n.486+274T>C |