Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.31667469C>T , CM000683.2:g.31667469C>T | GRCh38 |
| NC_000021.8:g.33039782C>T , CM000683.1:g.33039782C>T | GRCh37 |
| NC_000021.7:g.31961653C>T | NCBI36 |
| NG_008689.1:g.12848C>T , LRG_652:g.12848C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270142.11:c.357+94C>T MANE Select | ENSP00000270142.7:n.357+94C>T | |
| ENST00000270142.10:c.357+94C>T | ENSP00000270142.6:n.357+94C>T | |
| ENST00000389995.4:c.300+94C>T | ENSP00000374645.4:n.300+94C>T | |
| ENST00000470944.1:n.1285+94C>T | ||
| NM_000454.4:c.357+94C>T , LRG_652t1:c.357+94C>T | NP_000445.1:n.357+94C>T | |
| NM_000454.5:c.357+94C>T MANE Select | NP_000445.1:n.357+94C>T |