Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154837696C= , CM000685.2:g.154837696C= | GRCh38 |
| NC_000023.10:g.154065971C= , CM000685.1:g.154065971C= | GRCh37 |
| NC_000023.9:g.153719165C= | NCBI36 |
| NG_011403.1:g.190028G= | |
| NG_033065.1:g.1967G= | |
| NG_011403.2:g.190028G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000132.4:c.6957G= MANE Select | NP_000123.1:p.Pro2319= |
| ENST00000360256.9:c.6957G= MANE Select | ENSP00000353393.4:p.Pro2319= |
| NM_000132.3:c.6957G= | NP_000123.1:p.Pro2319= |
| NM_019863.2:c.552G= | NP_063916.1:p.Pro184= |
| NM_019863.3:c.552G= | NP_063916.1:p.Pro184= |
| ENST00000330287.10:c.552G= | ENSP00000327895.6:p.Pro184= |
| ENST00000360256.8:c.6957G= | ENSP00000353393.4:p.Pro2319= |
| ENST00000644698.1:c.690G= | ENSP00000495706.1:p.Pro230= |
| XM_011531126.1:c.6852G= | XP_011529428.1:p.Pro2284= |