Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128261743G= , CM000667.2:g.128261743G= | GRCh38 |
| NC_000005.9:g.127597435G= , CM000667.1:g.127597435G= | GRCh37 |
| NC_000005.8:g.127625334G= | NCBI36 |
| NG_008750.1:g.281301C= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000262464.9:c.8357C= MANE Select | ENSP00000262464.4:p.Pro2786= | |
| ENST00000262464.8:c.8357C= | ENSP00000262464.4:p.Pro2786= | |
| ENST00000508053.5:c.8357C= | ENSP00000424571.1:p.Pro2786= | |
| ENST00000619499.4:c.8354C= | ENSP00000482132.1:p.Pro2785= | |
| NM_001999.3:c.8357C= | NP_001990.2:p.Pro2786= | |
| XM_017009228.2:c.8204C= | XP_016864717.1:p.Pro2735= | |
| NM_001999.4:c.8357C= MANE Select | NP_001990.2:p.Pro2786= |