Linked Data
dbSNP Id:
rs559510605
gnomAD v2:
5-1415502-T-C
gnomAD v3:
5-1415387-T-C
gnomAD v4:
5-1415387-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1415387T>C , CM000667.2:g.1415387T>C | GRCh38 |
| NC_000005.9:g.1415502T>C , CM000667.1:g.1415502T>C | GRCh37 |
| NC_000005.8:g.1468502T>C | NCBI36 |
| NG_015885.1:g.35042A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270349.12:c.1032-572A>G MANE Select | ENSP00000270349.9:n.1032-572A>G | |
| ENST00000270349.11:c.1032-572A>G | ENSP00000270349.9:n.1032-572A>G | |
| ENST00000511750.1:n.482-572A>G | ||
| NM_001044.4:c.1032-572A>G | NP_001035.1:n.1032-572A>G | |
| NM_001044.5:c.1032-572A>G MANE Select | NP_001035.1:n.1032-572A>G |