Linked Data
gnomAD v4:
16-88719679-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.88719679C>T , CM000678.2:g.88719679C>T | GRCh38 |
| NC_000016.9:g.88786087C>T , CM000678.1:g.88786087C>T | GRCh37 |
| NC_000016.8:g.87313588C>T | NCBI36 |
| NG_042229.1:g.70542G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301015.14:c.6366G>A MANE Select | ENSP00000301015.9:p.Met2122Ile | |
| ENST00000466823.3:c.392G>A | ||
| ENST00000301015.13:c.6366G>A | ENSP00000301015.9:p.Met2122Ile | |
| ENST00000419505.5:c.132G>A | ENSP00000406358.1:p.Met44Ile | |
| ENST00000466823.2:c.392G>A | ||
| ENST00000495568.7:n.607G>A | ||
| ENST00000497793.2:n.521G>A | ||
| NM_001142864.2:c.6366G>A | NP_001136336.2:p.Met2122Ile | |
| NM_001142864.3:c.6366G>A | NP_001136336.2:p.Met2122Ile | |
| NM_001142864.4:c.6366G>A MANE Select | NP_001136336.2:p.Met2122Ile |