Linked Data
gnomAD v4:
6-32814229-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32814229G>T , CM000668.2:g.32814229G>T | GRCh38 |
| NC_000006.11:g.32782006G>T , CM000668.1:g.32782006G>T | GRCh37 |
| NC_000006.10:g.32889984G>T | NCBI36 |
| NG_009793.3:g.29542C>A | |
| NG_012008.1:g.7820C>A | |
| NG_009793.4:g.29542C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000438763.7:c.643+91C>A MANE Select | ENSP00000390020.2:n.643+91C>A | |
| ENST00000648009.1:c.643+91C>A | ENSP00000496848.1:n.643+91C>A | |
| ENST00000438763.6:c.643+91C>A | ENSP00000390020.2:n.643+91C>A | |
| ENST00000452392.2:c.2464+91C>A | ENSP00000391806.2:n.2464+91C>A | |
| ENST00000475235.1:n.771C>A | ||
| ENST00000488325.5:c.*414+91C>A | ENSP00000436618.1:n.*414+91C>A | |
| NM_002120.3:c.643+91C>A | NP_002111.1:n.643+91C>A | |
| NM_002120.4:c.643+91C>A MANE Select | NP_002111.1:n.643+91C>A |