Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.28161971T>C , CM000668.2:g.28161971T>C | GRCh38 |
| NC_000006.11:g.28129749T>C , CM000668.1:g.28129749T>C | GRCh37 |
| NC_000006.10:g.28237728T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000562227.2:n.53+150T>C | ||
| ENST00000440790.6:n.41+150T>C | ||
| ENST00000570126.1:n.30+150T>C | ||
| NR_103448.1:n.61+150T>C |