Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.14716572T>C , CM000667.2:g.14716572T>C | GRCh38 |
| NC_000005.9:g.14716681T>C , CM000667.1:g.14716681T>C | GRCh37 |
| NC_000005.8:g.14769681T>C | NCBI36 |
| NG_008273.1:g.160207A>G | |
| NG_008273.2:g.160214A>G | |
| NG_051625.1:g.60779T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000284268.8:c.1141+134A>G MANE Select | ENSP00000284268.6:n.1141+134A>G | |
| ENST00000284268.6:c.1141+134A>G | ENSP00000284268.6:n.1141+134A>G | |
| ENST00000502585.1:n.383+134A>G | ||
| NM_054027.4:c.1141+134A>G | NP_473368.1:n.1141+134A>G | |
| NM_054027.5:c.1141+134A>G | NP_473368.1:n.1141+134A>G | |
| XM_017009644.2:c.1057+134A>G | XP_016865133.1:n.1057+134A>G | |
| NM_054027.6:c.1141+134A>G MANE Select | NP_473368.1:n.1141+134A>G |