Linked Data
dbSNP Id:
rs754874846
ExAC:
2:176958408 G / A
gnomAD v2:
2-176958408-G-A
gnomAD v3:
2-176093680-G-A
gnomAD v4:
2-176093680-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.176093680G>A , CM000664.2:g.176093680G>A | GRCh38 |
| NC_000002.11:g.176958408G>A , CM000664.1:g.176958408G>A | GRCh37 |
| NC_000002.10:g.176666654G>A | NCBI36 |
| NG_008137.1:g.5877G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392539.4:c.781+9G>A MANE Select | ENSP00000376322.3:n.781+9G>A | |
| ENST00000392539.3:c.781+9G>A | ENSP00000376322.3:n.781+9G>A | |
| NM_000523.3:c.781+9G>A | NP_000514.2:n.781+9G>A | |
| XM_011511068.1:c.725-800G>A | XP_011509370.1:n.725-800G>A | |
| XM_011511068.2:c.725-800G>A | XP_011509370.1:n.725-800G>A | |
| NM_000523.4:c.781+9G>A MANE Select | NP_000514.2:n.781+9G>A |