Linked Data
dbSNP Id:
rs74007631
gnomAD v2:
16-11375371-C-A
gnomAD v3:
16-11281514-C-A
gnomAD v4:
16-11281514-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.11281514C>A , CM000678.2:g.11281514C>A | GRCh38 |
| NC_000016.9:g.11375371C>A , CM000678.1:g.11375371C>A | GRCh37 |
| NC_000016.8:g.11282872C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000649869.1:n.152+31736C>A | ||
| ENST00000572173.1:c.-515-13702C>A | ENSP00000461206.1:n.-515-13702C>A | |
| ENST00000573910.1:n.160+31736C>A | ||
| XR_933070.1:n.733+31736C>A | ||
| XR_933070.3:n.876+31736C>A |