Linked Data
dbSNP Id:
rs1416086132
gnomAD v2:
7-99367479-T-C
gnomAD v3:
7-99769856-T-C
gnomAD v4:
7-99769856-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.99769856T>C , CM000669.2:g.99769856T>C | GRCh38 |
| NC_000007.13:g.99367479T>C , CM000669.1:g.99367479T>C | GRCh37 |
| NC_000007.12:g.99205415T>C | NCBI36 |
| NG_008421.1:g.19330A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000336411.7:c.433A>G | ENSP00000337915.3:p.Met145Val | |
| ENST00000651514.1:c.433A>G MANE Select | ENSP00000498939.1:p.Met145Val | |
| ENST00000651783.1:c.58-1349A>G | ENSP00000498924.1:n.58-1349A>G | |
| ENST00000652018.1:c.286A>G | ENSP00000498733.1:p.Met96Val | |
| ENST00000336411.6:c.433A>G | ENSP00000337915.2:p.Met145Val | |
| ENST00000354593.6:c.72-1354A>G | ENSP00000346607.2:n.72-1354A>G | |
| ENST00000480043.1:n.330A>G | ||
| NM_001202855.2:c.433A>G | NP_001189784.1:p.Met145Val | |
| NM_017460.5:c.433A>G | NP_059488.2:p.Met145Val | |
| XM_011515841.1:c.433A>G | XP_011514143.1:p.Met145Val | |
| XM_011515842.1:c.433A>G | XP_011514144.1:p.Met145Val | |
| NM_017460.6:c.433A>G MANE Select | NP_059488.2:p.Met145Val | |
| NM_001202855.3:c.433A>G | NP_001189784.1:p.Met145Val |