Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.35823900T= , CM000668.2:g.35823900T= | GRCh38 |
| NC_000006.11:g.35791677T= , CM000668.1:g.35791677T= | GRCh37 |
| NC_000006.10:g.35899655T= | NCBI36 |
| NG_012184.1:g.23607T= | |
| NG_012184.2:g.23607T= | |
| NG_012184.3:g.31695T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360215.3:c.*935T= MANE Select | ENSP00000353346.1:n.*935T= | |
| ENST00000496656.2:n.578+4080T= | ||
| ENST00000651132.1:c.*935T= | ENSP00000498322.1:n.*935T= | |
| ENST00000651676.1:c.*16+4437T= | ENSP00000498699.1:n.*16+4437T= | |
| ENST00000652718.1:c.508+4437T= | ENSP00000498866.1:n.508+4437T= | |
| ENST00000360215.2:c.*935T= | ENSP00000353346.1:n.*935T= | |
| ENST00000496656.1:n.812+4080T= | ||
| NM_182548.3:c.*935T= | NP_872354.1:n.*935T= | |
| NM_182548.4:c.*935T= MANE Select | NP_872354.1:n.*935T= |