Linked Data
ClinVar Variation Id:
550649
ClinVar RCV Id:
RCV000665450
dbSNP Id:
rs901732635
gnomAD v4:
4-186284173-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186284173A>C , CM000666.2:g.186284173A>C | GRCh38 |
| NC_000004.11:g.187205327A>C , CM000666.1:g.187205327A>C | GRCh37 |
| NC_000004.10:g.187442321A>C | NCBI36 |
| NG_008051.1:g.23210A>C , LRG_583:g.23210A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000403665.7:c.1217A>C MANE Select | ENSP00000384957.2:p.His406Pro | |
| ENST00000264692.8:c.1055A>C | ENSP00000264692.5:p.His352Pro | |
| ENST00000403665.6:c.1217A>C | ENSP00000384957.2:p.His406Pro | |
| NM_000128.3:c.1217A>C , LRG_583t1:c.1217A>C | NP_000119.1:p.His406Pro | |
| XM_005262821.2:c.1220A>C | XP_005262878.1:p.His407Pro | |
| XM_005262822.2:c.1220A>C | XP_005262879.1:p.His407Pro | |
| XM_005262823.2:c.950A>C | XP_005262880.1:p.His317Pro | |
| XM_005262824.1:c.1220A>C | XP_005262881.1:p.His407Pro | |
| XM_006714137.1:c.1172A>C | XP_006714200.1:p.His391Pro | |
| XR_938706.1:n.1625A>C | ||
| XR_938707.1:n.1625A>C | ||
| XM_005262821.4:c.1220A>C | XP_005262878.1:p.His407Pro | |
| XM_005262822.4:c.1220A>C | XP_005262879.1:p.His407Pro | |
| XM_005262823.4:c.950A>C | XP_005262880.1:p.His317Pro | |
| XM_006714137.3:c.1172A>C | XP_006714200.1:p.His391Pro | |
| XM_017007884.2:c.*2189A>C | XP_016863373.1:n.*2189A>C | |
| XR_001741172.2:n.1691A>C | ||
| NM_000128.4:c.1217A>C MANE Select | NP_000119.1:p.His406Pro |