Linked Data
dbSNP Id:
rs1752908624
gnomAD v3:
5-151851468-A-C
gnomAD v4:
5-151851468-A-C
MyVariant Identifiers:
chr5:g.151231029A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.151851468A>C , CM000667.2:g.151851468A>C | GRCh38 |
| NC_000005.9:g.151231029A>C , CM000667.1:g.151231029A>C | GRCh37 |
| NC_000005.8:g.151211222A>C | NCBI36 |
| NG_011764.1:g.78369T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274576.9:c.834T>G MANE Select | ENSP00000274576.5:p.Pro278= | |
| ENST00000274576.8:c.834T>G | ENSP00000274576.4:p.Pro278= | |
| ENST00000455880.2:c.834T>G | ENSP00000411593.2:p.Pro278= | |
| ENST00000462581.6:c.*592T>G | ENSP00000430595.1:n.*592T>G | |
| ENST00000471351.2:n.1117T>G | ||
| NM_000171.3:c.834T>G | NP_000162.2:p.Pro278= | |
| NM_001146040.1:c.834T>G | NP_001139512.1:p.Pro278= | |
| NM_001292000.1:c.585T>G | NP_001278929.1:p.Pro195= | |
| XM_005268412.2:c.834T>G | XP_005268469.1:p.Pro278= | |
| NM_000171.4:c.834T>G MANE Select | NP_000162.2:p.Pro278= | |
| NM_001146040.2:c.834T>G | NP_001139512.1:p.Pro278= | |
| NM_001292000.2:c.585T>G | NP_001278929.1:p.Pro195= |