Linked Data
dbSNP Id:
rs1423434945
gnomAD v2:
7-150883881-C-A
gnomAD v3:
7-151186794-C-A
gnomAD v4:
7-151186794-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.151186794C>A , CM000669.2:g.151186794C>A | GRCh38 |
| NC_000007.13:g.150883881C>A , CM000669.1:g.150883881C>A | GRCh37 |
| NC_000007.12:g.150514814C>A | NCBI36 |
| NG_017016.1:g.6039G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000420175.3:c.316+21G>T MANE Select | ENSP00000391137.2:n.316+21G>T | |
| ENST00000275838.5:c.316+21G>T | ENSP00000275838.1:n.316+21G>T | |
| ENST00000377867.7:c.272-135G>T | ENSP00000367098.3:n.272-135G>T | |
| ENST00000415615.1:c.*360+21G>T | ENSP00000410871.1:n.*360+21G>T | |
| ENST00000420175.2:c.316+21G>T | ENSP00000391137.2:n.316+21G>T | |
| NM_001142459.1:c.316+21G>T | NP_001135931.2:n.316+21G>T | |
| NM_001142460.1:c.316+21G>T | NP_001135932.2:n.316+21G>T | |
| NM_080871.3:c.272-135G>T | NP_543147.2:n.272-135G>T | |
| XM_005249949.3:c.451+21G>T | XP_005250006.1:n.451+21G>T | |
| NM_001142459.2:c.316+21G>T MANE Select | NP_001135931.2:n.316+21G>T | |
| NM_080871.4:c.272-135G>T | NP_543147.2:n.272-135G>T |