Canonical Allele Identifier:
CA2676266910
Gene:
Linked Data
gnomAD v4:
5-159333155-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.159333155G>T , CM000667.2:g.159333155G>T | GRCh38 |
| NC_000005.9:g.158760163G>T , CM000667.1:g.158760163G>T | GRCh37 |
| NC_000005.8:g.158692741G>T | NCBI36 |
| NG_009618.1:g.2319C>A , LRG_71:g.2319C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_037889.1:n.745+152G>T |