Linked Data
ClinVar Variation Id:
349299
dbSNP Id:
rs886059523
gnomAD v2:
4-6271642-T-G
gnomAD v3:
4-6269915-T-G
gnomAD v4:
4-6269915-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.6269915T>G , CM000666.2:g.6269915T>G | GRCh38 |
| NC_000004.11:g.6271642T>G , CM000666.1:g.6271642T>G | GRCh37 |
| NC_000004.10:g.6322543T>G | NCBI36 |
| NG_011700.1:g.5066T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000506588.6:n.66T>G | ||
| ENST00000682275.1:c.-105T>G | ENSP00000507852.1:n.-105T>G | |
| ENST00000673991.1:c.-101T>G | ENSP00000501033.1:n.-101T>G | |
| ENST00000226760.5:c.-105T>G MANE Select | ENSP00000226760.1:n.-105T>G | |
| ENST00000503569.5:c.-101T>G | ENSP00000423337.1:n.-101T>G | |
| ENST00000506588.5:n.66T>G | ||
| NM_001145853.1:c.-101T>G | NP_001139325.1:n.-101T>G | |
| NM_006005.3:c.-105T>G MANE Select | NP_005996.2:n.-105T>G | |
| XM_017008586.1:c.5-7536T>G | XP_016864075.1:n.5-7536T>G |