Linked Data
dbSNP Id:
rs1334851277
gnomAD v2:
16-223339-G-A
gnomAD v3:
16-173340-G-A
gnomAD v4:
16-173340-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.173340G>A , CM000678.2:g.173340G>A | GRCh38 |
| NC_000016.9:g.223339G>A , CM000678.1:g.223339G>A | GRCh37 |
| NC_000016.8:g.163339G>A | NCBI36 |
| NG_000006.1:g.34203G>A | |
| NG_059186.1:g.1690G>A | |
| NG_059271.1:g.5494G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251595.11:c.300+11G>A MANE Select | ENSP00000251595.6:n.300+11G>A | |
| ENST00000251595.10:c.300+11G>A | ENSP00000251595.6:n.300+11G>A | |
| ENST00000397806.1:c.204+11G>A | ENSP00000380908.1:n.204+11G>A | |
| ENST00000482565.1:n.436+11G>A | ||
| ENST00000484216.1:n.280G>A | ||
| NM_000517.4:c.300+11G>A | NP_000508.1:n.300+11G>A | |
| NM_000517.6:c.300+11G>A MANE Select | NP_000508.1:n.300+11G>A |