Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.91950126A>G , CM000671.2:g.91950126A>G | GRCh38 |
| NC_000009.11:g.94712408A>G , CM000671.1:g.94712408A>G | GRCh37 |
| NC_000009.10:g.93752229A>G | NCBI36 |
| NG_008089.1:g.5037T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375708.4:c.-163T>C MANE Select | ENSP00000364860.3:n.-163T>C | |
| ENST00000375708.3:c.-163T>C | ENSP00000364860.3:n.-163T>C | |
| NM_004560.3:c.-163T>C | NP_004551.2:n.-163T>C | |
| NM_001318204.1:c.-163T>C | NP_001305133.1:n.-163T>C | |
| XR_001746315.1:n.81T>C | ||
| NM_004560.4:c.-163T>C MANE Select | NP_004551.2:n.-163T>C | |
| NM_001318204.2:c.-163T>C | NP_001305133.1:n.-163T>C |