Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38408900A= , CM000685.2:g.38408900A= | GRCh38 |
| NC_000023.10:g.38268153A= , CM000685.1:g.38268153A= | GRCh37 |
| NC_000023.9:g.38153097A= | NCBI36 |
| NG_008471.1:g.61418A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000039007.5:c.742A= MANE Select | ENSP00000039007.4:p.Asn248= | |
| ENST00000643344.1:c.*492A= | ENSP00000496606.1:n.*492A= | |
| ENST00000039007.4:c.742A= | ENSP00000039007.4:p.Asn248= | |
| ENST00000465127.1:c.172-257221A= | ENSP00000417050.1:n.172-257221A= | |
| NM_000531.5:c.742A= | NP_000522.3:p.Asn248= | |
| XM_017029556.1:c.742A= | XP_016885045.1:p.Asn248= | |
| NM_000531.6:c.742A= MANE Select | NP_000522.3:p.Asn248= |