dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94087882C>G , CM000663.2:g.94087882C>G | GRCh38 |
| NC_000001.10:g.94553438C>G , CM000663.1:g.94553438C>G | GRCh37 |
| NC_000001.9:g.94326026C>G | NCBI36 |
| NG_009073.1:g.38268G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.769-4441G>C MANE Select | ENSP00000359245.3:n.769-4441G>C | |
| ENST00000649773.1:c.769-4441G>C | ENSP00000496882.1:n.769-4441G>C | |
| ENST00000370225.3:c.769-4441G>C | ENSP00000359245.3:n.769-4441G>C | |
| NM_000350.2:c.769-4441G>C | NP_000341.2:n.769-4441G>C | |
| NM_000350.3:c.769-4441G>C MANE Select | NP_000341.2:n.769-4441G>C |