Linked Data
dbSNP Id:
rs781264248
ExAC:
15:40698044 C / T
gnomAD v2:
15-40698044-C-T
gnomAD v4:
15-40405843-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.40405843C>T , CM000677.2:g.40405843C>T | GRCh38 |
| NC_000015.9:g.40698044C>T , CM000677.1:g.40698044C>T | GRCh37 |
| NC_000015.8:g.38485336C>T | NCBI36 |
| NG_011986.1:g.5359C>T | |
| NG_011986.2:g.5359C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000479013.7:c.16C>T | ENSP00000417990.3:p.Arg6Trp | |
| ENST00000487418.8:c.16C>T MANE Select | ENSP00000418397.3:p.Arg6Trp | |
| ENST00000610693.5:c.16C>T | ENSP00000479359.2:p.Arg6Trp | |
| ENST00000650656.1:c.25C>T | ENSP00000498731.1:p.Arg9Trp | |
| ENST00000651168.1:c.25C>T | ENSP00000499074.1:p.Arg9Trp | |
| ENST00000479013.6:c.25C>T | ENSP00000417990.2:p.Arg9Trp | |
| ENST00000487418.6:c.25C>T | ENSP00000418397.2:p.Arg9Trp | |
| ENST00000610693.4:c.25C>T | ENSP00000479359.1:p.Arg9Trp | |
| NM_001159508.1:c.25C>T | NP_001152980.1:p.Arg9Trp | |
| NM_002225.3:c.25C>T | NP_002216.2:p.Arg9Trp | |
| XM_005254350.2:c.25C>T | XP_005254407.1:p.Arg9Trp | |
| XM_005254356.2:c.25C>T | XP_005254413.1:p.Arg9Trp | |
| XM_006720492.2:c.25C>T | XP_006720555.1:p.Arg9Trp | |
| XM_006720493.2:c.25C>T | XP_006720556.1:p.Arg9Trp | |
| XM_006720494.2:c.25C>T | XP_006720557.1:p.Arg9Trp | |
| XM_006720495.2:c.25C>T | XP_006720558.1:p.Arg9Trp | |
| XM_011521523.1:c.25C>T | XP_011519825.1:p.Arg9Trp | |
| XM_011521524.1:c.25C>T | XP_011519826.1:p.Arg9Trp | |
| XR_243097.3:n.25C>T | ||
| XR_243098.2:n.25C>T | ||
| XR_429453.2:n.126C>T | ||
| NM_001159508.2:c.16C>T | NP_001152980.2:p.Arg6Trp | |
| NM_001354597.2:c.-412C>T | NP_001341526.1:n.-412C>T | |
| NM_001354598.2:c.16C>T | NP_001341527.2:p.Arg6Trp | |
| NM_001354599.2:c.16C>T | NP_001341528.2:p.Arg6Trp | |
| NM_001354600.2:c.16C>T | NP_001341529.2:p.Arg6Trp | |
| NM_001354601.2:c.16C>T | NP_001341530.2:p.Arg6Trp | |
| NM_002225.4:c.16C>T | NP_002216.3:p.Arg6Trp | |
| NR_148925.1:n.47C>T | ||
| XM_006720495.3:c.25C>T | XP_006720558.1:p.Arg9Trp | |
| XM_017022149.1:c.25C>T | XP_016877638.1:p.Arg9Trp | |
| XM_017022150.1:c.25C>T | XP_016877639.1:p.Arg9Trp | |
| XM_017022153.1:c.25C>T | XP_016877642.1:p.Arg9Trp | |
| XM_017022155.2:c.25C>T | XP_016877644.1:p.Arg9Trp | |
| XM_017022157.1:c.25C>T | XP_016877646.1:p.Arg9Trp | |
| XM_017022158.2:c.25C>T | XP_016877647.1:p.Arg9Trp | |
| XR_001751264.1:n.37C>T | ||
| NM_001159508.3:c.16C>T | NP_001152980.2:p.Arg6Trp | |
| NM_001354597.3:c.-412C>T | NP_001341526.1:n.-412C>T | |
| NM_001354598.3:c.16C>T | NP_001341527.2:p.Arg6Trp | |
| NM_001354599.3:c.16C>T | NP_001341528.2:p.Arg6Trp | |
| NM_001354600.3:c.16C>T | NP_001341529.2:p.Arg6Trp | |
| NM_001354601.3:c.16C>T | NP_001341530.2:p.Arg6Trp | |
| NM_002225.5:c.16C>T MANE Select | NP_002216.3:p.Arg6Trp | |
| NR_148925.2:n.49C>T |