Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.98542180T>G , CM000671.2:g.98542180T>G | GRCh38 |
| NC_000009.11:g.101304462T>G , CM000671.1:g.101304462T>G | GRCh37 |
| NC_000009.10:g.100344283T>G | NCBI36 |
| NG_016426.1:g.172018A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259455.4:c.460-137A>C MANE Select | ENSP00000259455.2:n.460-137A>C | |
| ENST00000637410.1:n.238-137A>C | ||
| ENST00000637717.1:c.76-137A>C | ENSP00000490789.1:n.76-137A>C | |
| ENST00000638001.1:n.70-137A>C | ||
| ENST00000259455.3:c.460-137A>C | ENSP00000259455.2:n.460-137A>C | |
| ENST00000477471.1:n.247-137A>C | ||
| ENST00000634227.1:n.234-137A>C | ||
| NM_005458.7:c.460-137A>C | NP_005449.5:n.460-137A>C | |
| XM_017015331.2:c.166-137A>C | XP_016870820.1:n.166-137A>C | |
| NM_005458.8:c.460-137A>C MANE Select | NP_005449.5:n.460-137A>C |