Linked Data
dbSNP Id:
rs914174268
gnomAD v3:
16-68737257-G-A
gnomAD v4:
16-68737257-G-A
MyVariant Identifiers:
chr16:g.68737257G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.68737257G>A , CM000678.2:g.68737257G>A | GRCh38 |
| NC_000016.9:g.68771160G>A , CM000678.1:g.68771160G>A | GRCh37 |
| NC_000016.8:g.67328661G>A | NCBI36 |
| NG_008021.1:g.4966G>A , LRG_301:g.4966G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261769.9:c.-159G>A | ENSP00000261769.4:n.-159G>A |