Linked Data
dbSNP Id:
rs1326485315
gnomAD v3:
7-142753661-C-CTTTTTTAATG
gnomAD v4:
7-142753661-C-CTTTTTTAATG
MyVariant Identifiers:
chr7:g.142461512_142461513insTTTTTTAATG (hg19)
chr7:g.142753661_142753662insTTTTTTAATG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.142753661_142753662insTTTTTTAATG , CM000669.2:g.142753661_142753662insTTTTTTAATG | GRCh38 |
| NC_000007.13:g.142461512_142461513insTTTTTTAATG , CM000669.1:g.142461512_142461513insTTTTTTAATG | GRCh37 |
| NC_000007.12:g.142141086_142141087insTTTTTTAATG | NCBI36 |
| NG_008307.3:g.9178_9179insTTTTTTAATG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000610416.2:c.370+32475_370+32476insTTTTTTAATG (TRBC1) | ENSP00000482915.1:n.370+32475_370+32476insTTTTTTAATG | |
| ENST00000612126.4:c.591+1094_591+1095insTTTTTTAATG (PRSS1) | ENSP00000479959.1:n.591+1094_591+1095insTTTTTTAATG | |
| ENST00000633114.1:c.321+1767_321+1768insTTTTTTAATG (PRSS2) | ENSP00000487822.1:n.321+1767_321+1768insTTTTTTAATG | |
| ENST00000634019.1:c.82+4870_82+4871insTTTTTTAATG (PRSS2) | ENSP00000488594.1:n.82+4870_82+4871insTTTTTTAATG |