dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.119032590G>C , CM000670.2:g.119032590G>C | GRCh38 |
| NC_000008.10:g.120044829G>C , CM000670.1:g.120044829G>C | GRCh37 |
| NC_000008.9:g.120114010G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000521788.1:n.235+23037G>C | ||
| XM_005250756.2:c.-59-57090G>C | XP_005250813.1:n.-59-57090G>C | |
| NM_001324095.1:c.-323-4846G>C | NP_001311024.1:n.-323-4846G>C | |
| XM_005250756.3:c.-59-57090G>C | XP_005250813.1:n.-59-57090G>C | |
| NM_001324095.2:c.-323-4846G>C | NP_001311024.1:n.-323-4846G>C |