Linked Data
gnomAD v4:
5-136046073-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.136046073G>T , CM000667.2:g.136046073G>T | GRCh38 |
| NC_000005.9:g.135381762G>T , CM000667.1:g.135381762G>T | GRCh37 |
| NC_000005.8:g.135409661G>T | NCBI36 |
| NG_012646.1:g.22179G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000442011.7:c.299-262G>T MANE Select | ENSP00000416330.2:n.299-262G>T | |
| ENST00000442011.6:c.299-262G>T | ENSP00000416330.2:n.299-262G>T | |
| ENST00000504185.5:n.456-262G>T | ||
| ENST00000506699.5:n.364-262G>T | ||
| ENST00000507018.5:c.216-262G>T | ||
| ENST00000515433.1:n.329G>T | ||
| NM_000358.2:c.299-262G>T | NP_000349.1:n.299-262G>T | |
| NM_000358.3:c.299-262G>T MANE Select | NP_000349.1:n.299-262G>T |