Linked Data
gnomAD v4:
5-1416042-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1416042C>G , CM000667.2:g.1416042C>G | GRCh38 |
| NC_000005.9:g.1416157C>G , CM000667.1:g.1416157C>G | GRCh37 |
| NC_000005.8:g.1469157C>G | NCBI36 |
| NG_015885.1:g.34387G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270349.12:c.1031+56G>C MANE Select | ENSP00000270349.9:n.1031+56G>C | |
| ENST00000270349.11:c.1031+56G>C | ENSP00000270349.9:n.1031+56G>C | |
| ENST00000511750.1:n.481+56G>C | ||
| NM_001044.4:c.1031+56G>C | NP_001035.1:n.1031+56G>C | |
| NM_001044.5:c.1031+56G>C MANE Select | NP_001035.1:n.1031+56G>C |