Linked Data
dbSNP Id:
rs536694364
gnomAD v2:
5-110407356-A-T
gnomAD v3:
5-111071658-A-T
gnomAD v4:
5-111071658-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.111071658A>T , CM000667.2:g.111071658A>T | GRCh38 |
| NC_000005.9:g.110407356A>T , CM000667.1:g.110407356A>T | GRCh37 |
| NC_000005.8:g.110435255A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000420978.6:c.34+141A>T | ENSP00000399099.2:n.34+141A>T | |
| NR_045089.1:n.1438+141A>T | ||
| NR_045089.2:n.1456+141A>T |