HGVS | Genome Assembly |
---|---|
NC_000011.10:g.22625368A>G , CM000673.2:g.22625368A>G | GRCh38 |
NC_000011.9:g.22646914A>G , CM000673.1:g.22646914A>G | GRCh37 |
NC_000011.8:g.22603490A>G | NCBI36 |
NG_007425.1:g.5474T>C , LRG_527:g.5474T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327470.6:c.443T>C MANE Select | ENSP00000330875.3:p.Phe148Ser | |
ENST00000327470.4:c.443T>C | ENSP00000330875.3:p.Phe148Ser | |
NM_022725.3:c.443T>C , LRG_527t1:c.443T>C | NP_073562.1:p.Phe148Ser | |
NM_022725.4:c.443T>C MANE Select | NP_073562.1:p.Phe148Ser |