Linked Data
ClinVar Variation Id:
654211
dbSNP Id:
rs765445413
ExAC:
1:173881112 T / G
gnomAD v2:
1-173881112-T-G
gnomAD v3:
1-173911974-T-G
gnomAD v4:
1-173911974-T-G
ERepo:
CA1251409/MONDO:0013144/084
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.173911974T>G , CM000663.2:g.173911974T>G | GRCh38 |
| NC_000001.10:g.173881112T>G , CM000663.1:g.173881112T>G | GRCh37 |
| NC_000001.9:g.172147735T>G | NCBI36 |
| NG_012462.1:g.10405A>C , LRG_577:g.10405A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367698.4:c.449A>C MANE Select | ENSP00000356671.3:p.Gln150Pro | |
| ENST00000367698.3:c.449A>C | ENSP00000356671.3:p.Gln150Pro | |
| ENST00000487183.1:n.154A>C | ||
| ENST00000617423.4:c.449A>C | ENSP00000478688.1:p.Gln150Pro | |
| NM_000488.3:c.449A>C , LRG_577t1:c.449A>C | NP_000479.1:p.Gln150Pro | |
| XM_005245198.2:c.305A>C | XP_005245255.1:p.Gln102Pro | |
| NM_001365052.1:c.305A>C | NP_001351981.1:p.Gln102Pro | |
| NM_000488.4:c.449A>C MANE Select | NP_000479.1:p.Gln150Pro | |
| NM_001365052.2:c.305A>C | NP_001351981.1:p.Gln102Pro | |
| NM_001386302.1:c.449A>C | NP_001373231.1:p.Gln150Pro | |
| NM_001386303.1:c.530A>C | NP_001373232.1:p.Gln177Pro | |
| NM_001386304.1:c.449A>C | NP_001373233.1:p.Gln150Pro | |
| NM_001386305.1:c.449A>C | NP_001373234.1:p.Gln150Pro | |
| NM_001386306.1:c.409-1083A>C | NP_001373235.1:n.409-1083A>C |