Linked Data
dbSNP Id:
rs759555588
ExAC:
10:54531288 A / C
gnomAD v2:
10-54531288-A-C
gnomAD v3:
10-52771528-A-C
gnomAD v4:
10-52771528-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.52771528A>C , CM000672.2:g.52771528A>C | GRCh38 |
| NC_000010.10:g.54531288A>C , CM000672.1:g.54531288A>C | GRCh37 |
| NC_000010.9:g.54201294A>C | NCBI36 |
| NG_008196.1:g.5173T>G , LRG_154:g.5173T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000674931.1:c.108T>G MANE Select | ENSP00000502789.1:p.Ile36Met | |
| ENST00000675947.1:c.108T>G | ENSP00000502615.1:p.Ile36Met | |
| ENST00000373968.3:c.108T>G | ENSP00000363079.3:p.Ile36Met | |
| NM_000242.2:c.108T>G , LRG_154t1:c.108T>G | NP_000233.1:p.Ile36Met | |
| XM_006717861.2:c.108T>G | XP_006717924.1:p.Ile36Met | |
| XM_011539816.1:c.108T>G | XP_011538118.1:p.Ile36Met | |
| XM_006717861.4:c.108T>G | XP_006717924.1:p.Ile36Met | |
| XM_011539816.3:c.108T>G | XP_011538118.1:p.Ile36Met | |
| NM_000242.3:c.108T>G | NP_000233.1:p.Ile36Met | |
| NM_001378373.1:c.108T>G MANE Select | NP_001365302.1:p.Ile36Met | |
| NM_001378374.1:c.108T>G | NP_001365303.1:p.Ile36Met |