Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.57047054C= , CM000666.2:g.57047054C= | GRCh38 |
| NC_000004.11:g.57913220C= , CM000666.1:g.57913220C= | GRCh37 |
| NC_000004.10:g.57607977C= | NCBI36 |
| NG_031877.1:g.68332G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000295666.6:c.476-6121G= MANE Select | ENSP00000295666.4:n.476-6121G= | |
| ENST00000512512.3:n.116-6121G= | ||
| ENST00000514062.2:c.476-6121G= | ENSP00000486293.1:n.476-6121G= | |
| NM_001253835.1:c.476-6121G= | NP_001240764.1:n.476-6121G= | |
| NM_001553.2:c.476-6121G= | NP_001544.1:n.476-6121G= | |
| NM_001553.3:c.476-6121G= MANE Select | NP_001544.1:n.476-6121G= | |
| NM_001253835.2:c.476-6121G= | NP_001240764.1:n.476-6121G= |