Linked Data
dbSNP Id:
rs777327943
ExAC:
10:127477439 A / G
gnomAD v2:
10-127477439-A-G
gnomAD v4:
10-125788870-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.125788870A>G , CM000672.2:g.125788870A>G | GRCh38 |
| NC_000010.10:g.127477439A>G , CM000672.1:g.127477439A>G | GRCh37 |
| NC_000010.9:g.127467429A>G | NCBI36 |
| NG_011557.1:g.39399T>C | |
| NG_011557.2:g.39399T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000713579.1:c.796T>C | ENSP00000518871.1:p.Ter266Arg | |
| ENST00000368797.10:c.796T>C MANE Select | ENSP00000357787.4:p.Ter266Arg | |
| ENST00000465577.6:c.816T>C | ||
| ENST00000648427.1:c.*794T>C | ENSP00000497909.1:n.*794T>C | |
| ENST00000649536.1:c.796T>C | ENSP00000497817.1:p.Ter266Arg | |
| ENST00000650472.1:n.3182T>C | ||
| ENST00000650524.1:c.709T>C | ENSP00000498108.1:n.709T>C | |
| ENST00000650587.1:c.877T>C | ENSP00000497366.1:p.Ter293Arg | |
| ENST00000368786.5:c.796T>C | ENSP00000357775.1:p.Ter266Arg | |
| ENST00000368797.8:c.796T>C | ENSP00000357787.4:p.Ter266Arg | |
| ENST00000464267.1:n.893T>C | ||
| ENST00000465577.5:n.438T>C | ||
| ENST00000470483.1:n.484T>C | ||
| ENST00000484541.5:n.569T>C | ||
| ENST00000616800.4:c.161-3610T>C | ||
| ENST00000622016.4:c.241-3031T>C | ENSP00000483041.1:n.241-3031T>C | |
| NM_000375.2:c.796T>C | NP_000366.1:p.Ter266Arg | |
| XM_005270137.2:c.877T>C | XP_005270194.1:p.Ter293Arg | |
| XM_005270138.2:c.796T>C | XP_005270195.1:p.Ter266Arg | |
| XM_005270139.2:c.661-3031T>C | XP_005270196.1:n.661-3031T>C | |
| XM_006717960.2:c.877T>C | XP_006718023.1:p.Ter293Arg | |
| XM_011540127.1:c.661-3610T>C | XP_011538429.1:n.661-3610T>C | |
| XR_246103.2:n.976T>C | ||
| XR_945810.1:n.1206T>C | ||
| NM_000375.3:c.796T>C MANE Select | NP_000366.1:p.Ter266Arg | |
| NM_001324036.1:c.877T>C | NP_001310965.1:p.Ter293Arg | |
| NM_001324037.1:c.796T>C | NP_001310966.1:p.Ter266Arg | |
| NM_001324038.1:c.715T>C | NP_001310967.1:p.Ter239Arg | |
| NR_136675.1:n.881T>C | ||
| NR_136676.1:n.1308T>C | ||
| NR_136677.1:n.927-3031T>C | ||
| NR_136678.1:n.792T>C | ||
| XM_011540127.2:c.661-3610T>C | XP_011538429.1:n.661-3610T>C | |
| XM_017016611.2:c.877T>C | XP_016872100.2:p.Ter293Arg | |
| XM_017016612.2:c.661-3031T>C | XP_016872101.1:n.661-3031T>C | |
| XM_024448154.1:c.796T>C | XP_024303922.1:p.Ter266Arg | |
| XR_002957010.1:n.2135T>C | ||
| XR_246103.3:n.991T>C | ||
| XR_945810.2:n.1221T>C | ||
| NM_001324036.2:c.877T>C | NP_001310965.1:p.Ter293Arg | |
| NM_001324037.2:c.796T>C | NP_001310966.1:p.Ter266Arg | |
| NM_001324038.2:c.715T>C | NP_001310967.1:p.Ter239Arg | |
| NR_136675.2:n.871T>C | ||
| NR_136676.2:n.1298T>C | ||
| NR_136678.2:n.782T>C | ||
| NR_136677.2:n.917-3031T>C |