Linked Data
dbSNP Id:
rs11763469
gnomAD v2:
7-142482001-C-T
gnomAD v3:
7-142774142-C-T
gnomAD v4:
7-142774142-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.142774142C>T , CM000669.2:g.142774142C>T | GRCh38 |
| NC_000007.13:g.142482001C>T , CM000669.1:g.142482001C>T | GRCh37 |
| NC_000007.12:g.142181945C>T | NCBI36 |
| NG_008322.2:g.8200C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000539842.6:c.591+87C>T (PRSS2) MANE Select | ENSP00000488338.1:n.591+87C>T | |
| ENST00000539842.5:c.591+87C>T (PRSS2) | ENSP00000488338.1:n.591+87C>T | |
| ENST00000610416.2:c.371-12896C>T (TRBC1) | ENSP00000482915.1:n.371-12896C>T | |
| ENST00000618750.2:n.424+104C>T (PRSS2) | ||
| ENST00000632805.1:c.588+87C>T (PRSS2) | ENSP00000488077.1:n.588+87C>T | |
| ENST00000632998.1:c.591+87C>T (PRSS2) | ENSP00000488789.1:n.591+87C>T | |
| ENST00000633114.1:c.597+87C>T (PRSS2) | ENSP00000487822.1:n.597+87C>T | |
| ENST00000633969.1:c.633+87C>T (PRSS2) | ENSP00000488437.1:n.633+87C>T | |
| ENST00000634019.1:c.633+87C>T (PRSS2) | ENSP00000488594.1:n.633+87C>T | |
| NM_001303414.1:c.633+87C>T (PRSS2) | NP_001290343.1:n.633+87C>T | |
| NM_002770.3:c.591+87C>T (PRSS2) | NP_002761.1:n.591+87C>T | |
| NR_130149.1:n.557+87C>T (PRSS2) | ||
| NM_002770.4:c.591+87C>T (PRSS2) MANE Select | NP_002761.1:n.591+87C>T | |
| NR_130149.2:n.530+87C>T (PRSS2) | ||
| NM_001303414.2:c.633+87C>T (PRSS2) | NP_001290343.1:n.633+87C>T |