Linked Data
ClinVar Variation Id:
289702
dbSNP Id:
rs139664153
ExAC:
6:76623870 G / A
gnomAD v2:
6-76623870-G-A
gnomAD v3:
6-75914153-G-A
gnomAD v4:
6-75914153-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.75914153G>A , CM000668.2:g.75914153G>A | GRCh38 |
| NC_000006.11:g.76623870G>A , CM000668.1:g.76623870G>A | GRCh37 |
| NC_000006.10:g.76680590G>A | NCBI36 |
| NG_009934.1:g.169962G>A | |
| NG_009934.2:g.169961G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369975.6:c.3434G>A | ENSP00000358992.1:p.Arg1145His | |
| ENST00000369977.8:c.3530G>A MANE Select | ENSP00000358994.3:p.Arg1177His | |
| ENST00000369985.9:c.3461G>A | ENSP00000359002.3:p.Arg1154His | |
| ENST00000664640.1:c.3557G>A | ENSP00000499278.1:p.Arg1186His | |
| ENST00000671923.1:c.*1541G>A | ENSP00000500835.1:n.*1541G>A | |
| ENST00000672093.1:c.3530G>A | ENSP00000500710.1:p.Arg1177His | |
| ENST00000672162.1:n.1696G>A | ||
| ENST00000369975.5:c.3434G>A | ENSP00000358992.1:p.Arg1145His | |
| ENST00000369977.7:c.3530G>A | ENSP00000358994.3:p.Arg1177His | |
| ENST00000369981.7:c.3560G>A | ENSP00000358998.4:p.Arg1187His | |
| ENST00000369985.8:c.3461G>A | ENSP00000359002.3:p.Arg1154His | |
| ENST00000615563.4:c.3461G>A | ENSP00000478013.1:p.Arg1154His | |
| ENST00000627432.2:c.3557G>A | ENSP00000487348.1:p.Arg1186His | |
| NM_001300899.1:c.3461G>A | NP_001287828.1:p.Arg1154His | |
| NM_004999.3:c.3530G>A | NP_004990.3:p.Arg1177His | |
| XM_005248719.2:c.3557G>A | XP_005248776.1:p.Arg1186His | |
| XM_005248720.2:c.3530G>A | XP_005248777.1:p.Arg1177His | |
| XM_005248721.2:c.3518G>A | XP_005248778.1:p.Arg1173His | |
| XM_005248722.2:c.3503G>A | XP_005248779.1:p.Arg1168His | |
| XM_005248724.2:c.3491G>A | XP_005248781.1:p.Arg1164His | |
| XM_005248726.2:c.3434G>A | XP_005248783.1:p.Arg1145His | |
| XM_005248719.4:c.3557G>A | XP_005248776.1:p.Arg1186His | |
| XM_005248720.4:c.3530G>A | XP_005248777.1:p.Arg1177His | |
| XM_005248721.4:c.3518G>A | XP_005248778.1:p.Arg1173His | |
| XM_005248722.4:c.3503G>A | XP_005248779.1:p.Arg1168His | |
| XM_005248724.4:c.3491G>A | XP_005248781.1:p.Arg1164His | |
| XM_005248726.4:c.3434G>A | XP_005248783.1:p.Arg1145His | |
| XM_017010899.2:c.3464G>A | XP_016866388.1:p.Arg1155His | |
| XM_024446447.1:c.3557G>A | XP_024302215.1:p.Arg1186His | |
| XM_024446448.1:c.3491G>A | XP_024302216.1:p.Arg1164His | |
| NM_004999.4:c.3530G>A MANE Select | NP_004990.3:p.Arg1177His | |
| NM_001300899.2:c.3461G>A | NP_001287828.1:p.Arg1154His | |
| NM_001368136.1:c.3434G>A | NP_001355065.1:p.Arg1145His | |
| NM_001368137.1:c.3491G>A | NP_001355066.1:p.Arg1164His | |
| NM_001368138.1:c.3446G>A | NP_001355067.1:p.Arg1149His | |
| NM_001368865.1:c.3557G>A | NP_001355794.1:p.Arg1186His | |
| NM_001368866.1:c.3530G>A | NP_001355795.1:p.Arg1177His | |
| NR_160538.1:n.3759G>A |