dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.75483619G>T , CM000664.2:g.75483619G>T | GRCh38 |
| NC_000002.11:g.75710745G>T , CM000664.1:g.75710745G>T | GRCh37 |
| NC_000002.10:g.75564253G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000485891.1:n.411-14249C>A | ||
| ENST00000490746.5:n.521-14249C>A |