Linked Data
dbSNP Id:
rs11672691
gnomAD v3:
19-41479679-G-A
gnomAD v4:
19-41479679-G-A
MyVariant Identifiers:
chr19:g.41479679G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.41479679G>A , CM000681.2:g.41479679G>A | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_040109.1:n.950-395C>T | ||
| NR_040109.2:n.955-395C>T | ||
| NR_136334.1:n.67-395C>T |