Canonical Allele Identifier:
CA15126529
Gene:
Linked Data
dbSNP Id:
rs16834831
gnomAD v2:
1-192759186-T-G
gnomAD v3:
1-192790056-T-G
gnomAD v4:
1-192790056-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.192790056T>G , CM000663.2:g.192790056T>G | GRCh38 |
| NC_000001.10:g.192759186T>G , CM000663.1:g.192759186T>G | GRCh37 |
| NC_000001.9:g.191025809T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_922383.1:n.225+2243A>C | ||
| XR_922383.2:n.225+2243A>C |