Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.31668559T>G , CM000683.2:g.31668559T>G | GRCh38 |
| NC_000021.8:g.33040872T>G , CM000683.1:g.33040872T>G | GRCh37 |
| NC_000021.7:g.31962743T>G | NCBI36 |
| NG_008689.1:g.13938T>G , LRG_652:g.13938T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000454.5:c.446T>G MANE Select | NP_000445.1:p.Val149Gly |
| ENST00000270142.11:c.446T>G MANE Select | ENSP00000270142.7:p.Val149Gly |
| NM_000454.4:c.446T>G , LRG_652t1:c.446T>G | NP_000445.1:p.Val149Gly |
| ENST00000270142.10:c.446T>G | ENSP00000270142.6:p.Val149Gly |
| ENST00000389995.4:c.389T>G | ENSP00000374645.4:p.Val130Gly |
| ENST00000470944.1:n.1374T>G |