Linked Data
dbSNP Id:
rs887509155
gnomAD v2:
5-131755672-T-C
gnomAD v3:
5-132419980-T-C
gnomAD v4:
5-132419980-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.132419980T>C , CM000667.2:g.132419980T>C | GRCh38 |
| NC_000005.9:g.131755672T>C , CM000667.1:g.131755672T>C | GRCh37 |
| NC_000005.8:g.131783571T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000638452.2:c.-209+40T>C | ENSP00000492349.2:n.-209+40T>C | |
| ENST00000638504.1:n.206+40T>C | ||
| ENST00000638568.2:c.-351+40T>C | ENSP00000491158.2:n.-351+40T>C | |
| ENST00000639899.1:n.249+40T>C | ||
| ENST00000337752.6:c.48+40T>C (CARINH) | ENSP00000338228.2:n.48+40T>C | |
| ENST00000378947.7:c.48+40T>C (CARINH) | ENSP00000368230.3:n.48+40T>C | |
| ENST00000378953.8:c.48+40T>C (CARINH) | ENSP00000368236.4:n.48+40T>C | |
| ENST00000407797.5:c.48+40T>C (CARINH) | ENSP00000385513.1:n.48+40T>C | |
| ENST00000461203.5:n.179+40T>C (CARINH) | ||
| ENST00000621237.1:c.48+40T>C (CARINH) | ENSP00000481774.1:n.48+40T>C | |
| NR_045116.1:n.387+40T>C (CARINH) | ||
| NM_001207001.2:c.48+40T>C (CARINH) | NP_001193930.1:n.48+40T>C | |
| XR_948788.3:n.894-231A>G (LINC02863) | ||
| NR_161242.1:n.231+40T>C (CARINH) |