Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.31664085T= , CM000683.2:g.31664085T= | GRCh38 |
| NC_000021.8:g.33036398T= , CM000683.1:g.33036398T= | GRCh37 |
| NC_000021.7:g.31958269T= | NCBI36 |
| NG_008689.1:g.9464T= , LRG_652:g.9464T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270142.11:c.169+199T= MANE Select | ENSP00000270142.7:n.169+199T= | |
| ENST00000270142.10:c.169+199T= | ENSP00000270142.6:n.169+199T= | |
| ENST00000389995.4:c.112+199T= | ENSP00000374645.4:n.112+199T= | |
| ENST00000470944.1:n.1097+199T= | ||
| ENST00000476106.5:n.432+199T= | ||
| NM_000454.4:c.169+199T= , LRG_652t1:c.169+199T= | NP_000445.1:n.169+199T= | |
| NM_000454.5:c.169+199T= MANE Select | NP_000445.1:n.169+199T= |