Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.176119084C= , CM000664.2:g.176119084C= | GRCh38 |
| NC_000002.11:g.176983812C= , CM000664.1:g.176983812C= | GRCh37 |
| NC_000002.10:g.176692058C= | NCBI36 |
| NG_008133.2:g.12321C= , LRG_246:g.12321C= | |
| NG_009225.1:g.1400C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000249501.5:c.876C= MANE Select | ENSP00000249501.4:p.Thr292= | |
| ENST00000249501.4:c.876C= | ENSP00000249501.4:p.Thr292= | |
| ENST00000490088.2:n.700C= | ||
| ENST00000549469.1:n.747C= | ||
| NM_002148.3:c.876C= , LRG_246t1:c.876C= | NP_002139.2:p.Thr292= | |
| NM_002148.4:c.876C= MANE Select | NP_002139.2:p.Thr292= |