Linked Data
gnomAD v4:
6-38683090-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.38683090C>T , CM000668.2:g.38683090C>T | GRCh38 |
| NC_000006.11:g.38650866C>T , CM000668.1:g.38650866C>T | GRCh37 |
| NC_000006.10:g.38758844C>T | NCBI36 |
| NG_012074.1:g.25087G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373365.5:c.309-215G>A MANE Select | ENSP00000362463.3:n.309-215G>A | |
| ENST00000373365.4:c.309-215G>A | ENSP00000362463.3:n.309-215G>A | |
| ENST00000470973.1:n.126G>A | ||
| NM_006708.2:c.309-215G>A | NP_006699.2:n.309-215G>A | |
| NM_006708.3:c.309-215G>A MANE Select | NP_006699.2:n.309-215G>A |