HGVS | Genome Assembly |
---|---|
NC_000012.12:g.49951093T>C , CM000674.2:g.49951093T>C | GRCh38 |
NC_000012.11:g.50344876T>C , CM000674.1:g.50344876T>C | GRCh37 |
NC_000012.10:g.48631143T>C | NCBI36 |
NG_008913.1:g.5353T>C , LRG_717:g.5353T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000199280.4:c.263T>C MANE Select | ENSP00000199280.3:p.Phe88Ser | |
ENST00000199280.3:c.263T>C | ENSP00000199280.3:p.Phe88Ser | |
ENST00000550862.1:c.263T>C | ENSP00000450022.1:p.Phe88Ser | |
ENST00000551526.5:c.263T>C | ENSP00000447148.1:p.Phe88Ser | |
NM_000486.5:c.263T>C , LRG_717t1:c.263T>C | NP_000477.1:p.Phe88Ser | |
NM_000486.6:c.263T>C MANE Select | NP_000477.1:p.Phe88Ser |