Linked Data
dbSNP Id:
rs2127420337
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.49459029A>C , CM000668.2:g.49459029A>C | GRCh38 |
| NC_000006.11:g.49426742A>C , CM000668.1:g.49426742A>C | GRCh37 |
| NC_000006.10:g.49534701A>C | NCBI36 |
| NG_007100.1:g.9111T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274813.4:c.385+53T>G MANE Select | ENSP00000274813.3:n.385+53T>G | |
| ENST00000274813.3:c.385+53T>G | ENSP00000274813.3:n.385+53T>G | |
| NM_000255.3:c.385+53T>G | NP_000246.2:n.385+53T>G | |
| XM_005249143.2:c.385+53T>G | XP_005249200.1:n.385+53T>G | |
| XM_005249143.3:c.385+53T>G | XP_005249200.1:n.385+53T>G | |
| NM_000255.4:c.385+53T>G MANE Select | NP_000246.2:n.385+53T>G |