Linked Data
dbSNP Id:
rs761836004
gnomAD v2:
17-38028942-T-G
gnomAD v3:
17-39872689-T-G
gnomAD v4:
17-39872689-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.39872689T>G , CM000679.2:g.39872689T>G | GRCh38 |
| NC_000017.10:g.38028942T>G , CM000679.1:g.38028942T>G | GRCh37 |
| NC_000017.9:g.35282468T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000348931.9:c.625+201T>G MANE Select | ENSP00000335384.5:n.625+201T>G | |
| ENST00000348931.8:c.625+201T>G | ENSP00000335384.5:n.625+201T>G | |
| ENST00000377940.3:c.559+201T>G | ENSP00000367174.3:n.559+201T>G | |
| ENST00000583811.5:c.271+201T>G | ENSP00000462463.1:n.271+201T>G | |
| ENST00000584588.5:c.407-355T>G | ENSP00000462067.1:n.407-355T>G | |
| NM_198844.2:c.559+201T>G | NP_942141.2:n.559+201T>G | |
| NM_199321.2:c.625+201T>G | NP_955353.1:n.625+201T>G | |
| XM_011524298.1:c.625+201T>G | XP_011522600.1:n.625+201T>G | |
| XR_002957959.1:n.816+201T>G | ||
| NM_198844.3:c.559+201T>G | NP_942141.2:n.559+201T>G | |
| NM_199321.3:c.625+201T>G MANE Select | NP_955353.1:n.625+201T>G |