Linked Data
ClinVar Variation Id:
315282
dbSNP Id:
rs200745301
ExAC:
15:100657100 G / A
gnomAD v2:
15-100657100-G-A
gnomAD v3:
15-100116895-G-A
gnomAD v4:
15-100116895-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.100116895G>A , CM000677.2:g.100116895G>A | GRCh38 |
| NC_000015.9:g.100657100G>A , CM000677.1:g.100657100G>A | GRCh37 |
| NC_000015.8:g.98474623G>A | NCBI36 |
| NG_016287.1:g.230084C>T | |
| NG_016287.2:g.230084C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000268070.9:c.1840C>T MANE Select | ENSP00000268070.4:p.Arg614Trp | |
| ENST00000568565.2:c.1840C>T | ENSP00000456161.2:p.Arg614Trp | |
| ENST00000268070.8:c.1840C>T | ENSP00000268070.4:p.Arg614Trp | |
| ENST00000378898.8:n.1521C>T | ||
| NM_139057.2:c.1840C>T | NP_620688.2:p.Arg614Trp | |
| XM_005254872.2:c.1840C>T | XP_005254929.1:p.Arg614Trp | |
| XM_011521312.1:c.1840C>T | XP_011519614.1:p.Arg614Trp | |
| NM_139057.3:c.1840C>T | NP_620688.2:p.Arg614Trp | |
| XM_005254872.3:c.1840C>T | XP_005254929.1:p.Arg614Trp | |
| XM_011521312.2:c.1840C>T | XP_011519614.1:p.Arg614Trp | |
| XM_017021973.2:c.1972C>T | XP_016877462.1:p.Arg658Trp | |
| XM_017021974.1:c.1972C>T | XP_016877463.1:p.Arg658Trp | |
| XM_017021975.1:c.1972C>T | XP_016877464.1:p.Arg658Trp | |
| XM_017021976.1:c.1243C>T | XP_016877465.1:p.Arg415Trp | |
| XM_017021977.1:c.1972C>T | XP_016877466.1:p.Arg658Trp | |
| XM_017021978.1:c.874C>T | XP_016877467.1:p.Arg292Trp | |
| XM_017021979.1:c.652C>T | XP_016877468.1:p.Arg218Trp | |
| XM_017021980.1:c.652C>T | XP_016877469.1:p.Arg218Trp | |
| XM_017021981.1:c.1972C>T | XP_016877470.1:p.Arg658Trp | |
| XM_017021982.1:c.361C>T | XP_016877471.1:p.Arg121Trp | |
| XM_017021983.1:c.145C>T | XP_016877472.1:p.Arg49Trp | |
| XM_017021984.1:c.1111C>T | XP_016877473.1:p.Arg371Trp | |
| XR_001751118.1:n.2994C>T | ||
| XR_001751119.1:n.2994C>T | ||
| XR_001751120.1:n.2994C>T | ||
| NM_139057.4:c.1840C>T MANE Select | NP_620688.2:p.Arg614Trp |