Linked Data
dbSNP Id:
rs746168650
ExAC:
6:150710657 T / C
gnomAD v2:
6-150710657-T-C
gnomAD v4:
6-150389521-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.150389521T>C , CM000668.2:g.150389521T>C | GRCh38 |
| NC_000006.11:g.150710657T>C , CM000668.1:g.150710657T>C | GRCh37 |
| NC_000006.10:g.150752350T>C | NCBI36 |
| NG_016007.1:g.25630T>C | |
| NG_016007.2:g.25630T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000344419.8:c.348T>C MANE Select | ENSP00000343763.4:p.Ile116= | |
| ENST00000229447.9:c.348T>C | ENSP00000229447.5:p.Ile116= | |
| ENST00000344419.7:c.348T>C | ENSP00000343763.3:p.Ile116= | |
| ENST00000367335.7:c.348T>C | ENSP00000356304.3:p.Ile116= | |
| ENST00000392255.7:c.348T>C | ENSP00000376084.3:p.Ile116= | |
| ENST00000392256.6:c.348T>C | ENSP00000376085.2:p.Ile116= | |
| ENST00000422583.2:c.179+46T>C | ENSP00000397342.2:n.179+46T>C | |
| ENST00000425615.3:c.183T>C | ENSP00000390081.3:p.Ile61= | |
| ENST00000500320.7:c.348T>C | ENSP00000441276.1:p.Ile116= | |
| ENST00000546121.1:n.291T>C | ||
| NM_001164694.1:c.348T>C | NP_001158166.1:p.Ile116= | |
| NM_001164695.1:c.348T>C | NP_001158167.1:p.Ile116= | |
| NM_203395.2:c.348T>C | NP_981932.1:p.Ile116= | |
| XM_006715478.2:c.348T>C | XP_006715541.1:p.Ile116= | |
| XM_006715479.2:c.183T>C | XP_006715542.1:p.Ile61= | |
| XR_245516.3:n.511T>C | ||
| NM_001318495.1:c.124+46T>C | NP_001305424.1:n.124+46T>C | |
| NR_134655.1:n.488T>C | ||
| XM_006715478.3:c.348T>C | XP_006715541.1:p.Ile116= | |
| XM_006715479.3:c.183T>C | XP_006715542.1:p.Ile61= | |
| NM_001164694.2:c.348T>C | NP_001158166.1:p.Ile116= | |
| NM_001164695.2:c.348T>C | NP_001158167.1:p.Ile116= | |
| NM_001318495.2:c.124+46T>C | NP_001305424.1:n.124+46T>C | |
| NM_203395.3:c.348T>C MANE Select | NP_981932.1:p.Ile116= | |
| NR_134655.2:n.368T>C |