Linked Data
gnomAD v4:
5-136046531-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.136046531G>A , CM000667.2:g.136046531G>A | GRCh38 |
| NC_000005.9:g.135382220G>A , CM000667.1:g.135382220G>A | GRCh37 |
| NC_000005.8:g.135410119G>A | NCBI36 |
| NG_012646.1:g.22637G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000442011.7:c.459+36G>A MANE Select | ENSP00000416330.2:n.459+36G>A | |
| ENST00000442011.6:c.459+36G>A | ENSP00000416330.2:n.459+36G>A | |
| ENST00000506699.5:n.560G>A | ||
| ENST00000507018.5:c.412G>A | ||
| ENST00000515433.1:n.787G>A | ||
| NM_000358.2:c.459+36G>A | NP_000349.1:n.459+36G>A | |
| NM_000358.3:c.459+36G>A MANE Select | NP_000349.1:n.459+36G>A |