Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.86085031A>G , CM000671.2:g.86085031A>G | GRCh38 |
| NC_000009.11:g.88699946A>G , CM000671.1:g.88699946A>G | GRCh37 |
| NC_000009.10:g.87889766A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000388711.7:c.-21-5690T>C | ENSP00000373363.3:n.-21-5690T>C | |
| ENST00000388712.7:c.-21-5690T>C MANE Select | ENSP00000373364.3:n.-21-5690T>C | |
| ENST00000466178.1:c.-133T>C | ENSP00000418155.1:n.-133T>C | |
| ENST00000472919.1:n.150-5690T>C | ||
| NM_016548.3:c.-21-5690T>C | NP_057632.2:n.-21-5690T>C | |
| NM_177937.2:c.-21-5690T>C | NP_808800.1:n.-21-5690T>C | |
| NM_016548.4:c.-21-5690T>C MANE Select | NP_057632.2:n.-21-5690T>C | |
| NM_177937.3:c.-21-5690T>C | NP_808800.1:n.-21-5690T>C |