Linked Data
dbSNP Id:
rs1317564269
gnomAD v3:
13-19130985-A-C
gnomAD v4:
13-19130985-A-C
MyVariant Identifiers:
chr13:g.19705125A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.19130985A>C , CM000675.2:g.19130985A>C | GRCh38 |
| NC_000013.10:g.19705125A>C , CM000675.1:g.19705125A>C | GRCh37 |
| NC_000013.9:g.18603125A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000425713.1:n.493-307A>C |