Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128840198G= , CM000669.2:g.128840198G= | GRCh38 |
| NC_000007.13:g.128480252G= , CM000669.1:g.128480252G= | GRCh37 |
| NC_000007.12:g.128267488G= | NCBI36 |
| NG_011807.1:g.14770G= , LRG_870:g.14770G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000325888.13:c.1549+38G= MANE Select | ENSP00000327145.8:n.1549+38G= | |
| ENST00000325888.12:c.1549+38G= | ENSP00000327145.8:n.1549+38G= | |
| ENST00000346177.6:c.1549+38G= | ENSP00000344002.6:n.1549+38G= | |
| NM_001127487.1:c.1549+38G= | NP_001120959.1:n.1549+38G= | |
| NM_001458.4:c.1549+38G= , LRG_870t1:c.1549+38G= | NP_001449.3:n.1549+38G= | |
| NM_001127487.2:c.1549+38G= | NP_001120959.1:n.1549+38G= | |
| NM_001458.5:c.1549+38G= MANE Select | NP_001449.3:n.1549+38G= |