Linked Data
ClinVar Variation Id:
767265
ClinVar RCV Id:
RCV000945965
dbSNP Id:
rs144729918
ExAC:
5:7885816 T / C
gnomAD v2:
5-7885816-T-C
gnomAD v3:
5-7885703-T-C
gnomAD v4:
5-7885703-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.7885703T>C , CM000667.2:g.7885703T>C | GRCh38 |
| NC_000005.9:g.7885816T>C , CM000667.1:g.7885816T>C | GRCh37 |
| NC_000005.8:g.7938816T>C | NCBI36 |
| NG_008856.1:g.21600T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000440940.7:c.906T>C MANE Select | ENSP00000402510.2:p.Asn302= | |
| ENST00000264668.6:c.987T>C | ENSP00000264668.2:p.Asn329= | |
| ENST00000440940.6:c.906T>C | ENSP00000402510.2:p.Asn302= | |
| ENST00000508101.5:n.146T>C | ||
| ENST00000510525.5:c.931T>C | ||
| ENST00000511461.5:c.819T>C | ||
| ENST00000513439.5:c.*613T>C | ENSP00000426710.1:n.*613T>C | |
| NM_002454.2:c.906T>C | NP_002445.2:p.Asn302= | |
| NM_024010.2:c.987T>C | NP_076915.2:p.Asn329= | |
| XM_006714474.2:c.987T>C | XP_006714537.1:p.Asn329= | |
| XM_011514043.1:c.987T>C | XP_011512345.1:p.Asn329= | |
| XM_011514044.1:c.906T>C | XP_011512346.1:p.Asn302= | |
| XM_011514045.1:c.1127T>C | XP_011512347.1:p.Ile376Thr | |
| XR_241702.1:n.1009T>C | ||
| XR_241703.1:n.1002T>C | ||
| XR_925614.1:n.1009T>C | ||
| XR_925615.1:n.1009T>C | ||
| NM_001364440.1:c.906T>C | NP_001351369.1:p.Asn302= | |
| NM_001364441.1:c.906T>C | NP_001351370.1:p.Asn302= | |
| NM_001364442.1:c.906T>C | NP_001351371.1:p.Asn302= | |
| NM_024010.3:c.906T>C | NP_076915.3:p.Asn302= | |
| NR_134480.1:n.1029T>C | ||
| NR_134481.1:n.1043T>C | ||
| NR_134482.1:n.889T>C | ||
| NR_157168.1:n.959T>C | ||
| NR_157169.1:n.819T>C | ||
| NR_157170.1:n.985T>C | ||
| NR_157171.1:n.819T>C | ||
| NR_157172.1:n.845T>C | ||
| NR_157173.1:n.973T>C | ||
| NR_157174.1:n.845T>C | ||
| NR_157175.1:n.999T>C | ||
| NR_157176.1:n.1139T>C | ||
| NR_157177.1:n.994T>C | ||
| NR_157178.1:n.999T>C | ||
| XM_024446063.1:c.951T>C | XP_024301831.1:p.Asn317= | |
| XM_024446064.1:c.906T>C | XP_024301832.1:p.Asn302= | |
| XR_001742071.1:n.1009T>C | ||
| XR_001742072.1:n.1009T>C | ||
| XR_001742074.1:n.1009T>C | ||
| XR_001742075.1:n.1009T>C | ||
| XR_001742076.1:n.1149T>C | ||
| XR_001742077.1:n.1149T>C | ||
| NM_001364440.2:c.906T>C | NP_001351369.1:p.Asn302= | |
| NM_001364441.2:c.906T>C | NP_001351370.1:p.Asn302= | |
| NM_001364442.2:c.906T>C | NP_001351371.1:p.Asn302= | |
| NM_002454.3:c.906T>C MANE Select | NP_002445.2:p.Asn302= | |
| NM_024010.4:c.906T>C | NP_076915.3:p.Asn302= | |
| NR_134480.2:n.985T>C | ||
| NR_134481.2:n.999T>C | ||
| NR_134482.2:n.845T>C | ||
| NR_157168.2:n.959T>C | ||
| NR_157169.2:n.819T>C | ||
| NR_157170.2:n.985T>C | ||
| NR_157171.2:n.819T>C | ||
| NR_157172.2:n.845T>C | ||
| NR_157173.2:n.973T>C | ||
| NR_157174.2:n.845T>C | ||
| NR_157175.2:n.999T>C | ||
| NR_157176.2:n.1139T>C | ||
| NR_157177.2:n.994T>C | ||
| NR_157178.2:n.999T>C |