Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.31668548G>C , CM000683.2:g.31668548G>C | GRCh38 |
| NC_000021.8:g.33040861G>C , CM000683.1:g.33040861G>C | GRCh37 |
| NC_000021.7:g.31962732G>C | NCBI36 |
| NG_008689.1:g.13927G>C , LRG_652:g.13927G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000454.5:c.435G>C MANE Select | NP_000445.1:p.Leu145Phe |
| ENST00000270142.11:c.435G>C MANE Select | ENSP00000270142.7:p.Leu145Phe |
| NM_000454.4:c.435G>C , LRG_652t1:c.435G>C | NP_000445.1:p.Leu145Phe |
| ENST00000270142.10:c.435G>C | ENSP00000270142.6:p.Leu145Phe |
| ENST00000389995.4:c.378G>C | ENSP00000374645.4:p.Leu126Phe |
| ENST00000470944.1:n.1363G>C |