Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.151004695G>T , CM000669.2:g.151004695G>T | GRCh38 |
| NC_000007.13:g.150701783G>T , CM000669.1:g.150701783G>T | GRCh37 |
| NC_000007.12:g.150332716G>T | NCBI36 |
| NG_011992.1:g.18637G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000603.5:c.1753-1732G>T MANE Select | NP_000594.2:n.1753-1732G>T |
| ENST00000297494.8:c.1753-1732G>T MANE Select | ENSP00000297494.3:n.1753-1732G>T |
| NM_000603.4:c.1753-1732G>T | NP_000594.2:n.1753-1732G>T |
| ENST00000297494.7:c.1753-1732G>T | ENSP00000297494.3:n.1753-1732G>T |
| ENST00000461406.5:c.1135-1732G>T | ENSP00000417143.1:n.1135-1732G>T |
| XM_006716002.2:c.1753-1732G>T | XP_006716065.1:n.1753-1732G>T |