Linked Data
gnomAD v4:
1-206116707-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.206116707G>T , CM000663.2:g.206116707G>T | GRCh38 |
| NC_000001.10:g.206224624C>A , CM000663.1:g.206224624C>A | GRCh37 |
| NC_000001.9:g.204391247C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000367126.5:c.184C>A MANE Select | ENSP00000356094.4:p.Leu62Met | |
| ENST00000367126.4:c.184C>A | ENSP00000356094.4:p.Leu62Met | |
| ENST00000612906.1:n.36+957C>A | ||
| NM_000707.3:c.184C>A | NP_000698.1:p.Leu62Met | |
| NM_000707.4:c.184C>A | NP_000698.1:p.Leu62Met | |
| NM_000707.5:c.184C>A MANE Select | NP_000698.1:p.Leu62Met |