Linked Data
gnomAD v2:
16-223447-G-A
gnomAD v4:
16-173448-G-A
MyVariant Identifiers:
chr16:g.223447G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.173448G>A , CM000678.2:g.173448G>A | GRCh38 |
| NC_000016.9:g.223447G>A , CM000678.1:g.223447G>A | GRCh37 |
| NC_000016.8:g.163447G>A | NCBI36 |
| NG_000006.1:g.34311G>A | |
| NG_059186.1:g.1798G>A | |
| NG_059271.1:g.5602G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251595.11:c.301-24G>A MANE Select | ENSP00000251595.6:n.301-24G>A | |
| ENST00000251595.10:c.301-24G>A | ENSP00000251595.6:n.301-24G>A | |
| ENST00000397806.1:c.205-24G>A | ENSP00000380908.1:n.205-24G>A | |
| ENST00000482565.1:n.437-24G>A | ||
| ENST00000484216.1:n.388G>A | ||
| NM_000517.4:c.301-24G>A | NP_000508.1:n.301-24G>A | |
| NM_000517.6:c.301-24G>A MANE Select | NP_000508.1:n.301-24G>A |