Linked Data
dbSNP Id:
rs186884477
ExAC:
8:18257521 T / C
gnomAD v2:
8-18257521-T-C
gnomAD v3:
8-18400011-T-C
gnomAD v4:
8-18400011-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.18400011T>C , CM000670.2:g.18400011T>C | GRCh38 |
| NC_000008.10:g.18257521T>C , CM000670.1:g.18257521T>C | GRCh37 |
| NC_000008.9:g.18301801T>C | NCBI36 |
| NG_012246.1:g.13767T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286479.4:c.8T>C MANE Select | ENSP00000286479.3:p.Ile3Thr | |
| ENST00000286479.3:c.8T>C | ENSP00000286479.3:p.Ile3Thr | |
| ENST00000520116.1:c.-57-326T>C | ENSP00000428416.1:n.-57-326T>C | |
| NM_000015.2:c.8T>C | NP_000006.2:p.Ile3Thr | |
| XM_011544358.1:c.8T>C | XP_011542660.1:p.Ile3Thr | |
| XM_017012938.1:c.8T>C | XP_016868427.1:p.Ile3Thr | |
| NM_000015.3:c.8T>C MANE Select | NP_000006.2:p.Ile3Thr |