Linked Data
ClinVar Variation Id:
970521
ClinVar RCV Id:
RCV001246103
dbSNP Id:
rs1657788029
gnomAD v4:
1-173911938-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.173911938A>G , CM000663.2:g.173911938A>G | GRCh38 |
| NC_000001.10:g.173881076A>G , CM000663.1:g.173881076A>G | GRCh37 |
| NC_000001.9:g.172147699A>G | NCBI36 |
| NG_012462.1:g.10441T>C , LRG_577:g.10441T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000367698.4:c.485T>C MANE Select | ENSP00000356671.3:p.Leu162Pro | |
| ENST00000367698.3:c.485T>C | ENSP00000356671.3:p.Leu162Pro | |
| ENST00000487183.1:n.190T>C | ||
| ENST00000617423.4:c.485T>C | ENSP00000478688.1:p.Leu162Pro | |
| NM_000488.3:c.485T>C , LRG_577t1:c.485T>C | NP_000479.1:p.Leu162Pro | |
| XM_005245198.2:c.341T>C | XP_005245255.1:p.Leu114Pro | |
| NM_001365052.1:c.341T>C | NP_001351981.1:p.Leu114Pro | |
| NM_000488.4:c.485T>C MANE Select | NP_000479.1:p.Leu162Pro | |
| NM_001365052.2:c.341T>C | NP_001351981.1:p.Leu114Pro | |
| NM_001386302.1:c.485T>C | NP_001373231.1:p.Leu162Pro | |
| NM_001386303.1:c.566T>C | NP_001373232.1:p.Leu189Pro | |
| NM_001386304.1:c.485T>C | NP_001373233.1:p.Leu162Pro | |
| NM_001386305.1:c.485T>C | NP_001373234.1:p.Leu162Pro | |
| NM_001386306.1:c.409-1047T>C | NP_001373235.1:n.409-1047T>C |