dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.15672916G>C , CM000673.2:g.15672916G>C | GRCh38 |
| NC_000011.9:g.15694462G>C , CM000673.1:g.15694462G>C | GRCh37 |
| NC_000011.8:g.15651038G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NM_001293172.1:c.106+28881G>C | NP_001280101.1:n.106+28881G>C | |
| XM_011519838.1:c.106+28881G>C | XP_011518140.1:n.106+28881G>C | |
| XM_011519839.1:c.106+28881G>C | XP_011518141.1:n.106+28881G>C | |
| XM_011519838.3:c.106+28881G>C | XP_011518140.1:n.106+28881G>C | |
| XM_011519839.2:c.106+28881G>C | XP_011518141.1:n.106+28881G>C | |
| NR_169502.1:n.756+28881G>C | ||
| NR_169503.1:n.770+28881G>C | ||
| NR_169507.1:n.84-31417G>C | ||
| NR_169508.1:n.493+28881G>C | ||
| NR_169509.1:n.252+28881G>C |