Linked Data
gnomAD v4:
16-11281445-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.11281445T>C , CM000678.2:g.11281445T>C | GRCh38 |
| NC_000016.9:g.11375302T>C , CM000678.1:g.11375302T>C | GRCh37 |
| NC_000016.8:g.11282803T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000649869.1:n.152+31667T>C | ||
| ENST00000572173.1:c.-515-13771T>C | ENSP00000461206.1:n.-515-13771T>C | |
| ENST00000573910.1:n.160+31667T>C | ||
| XR_933070.1:n.733+31667T>C | ||
| XR_933070.3:n.876+31667T>C |