Linked Data
gnomAD v4:
X-136659265-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.136659265C>G , CM000685.2:g.136659265C>G | GRCh38 |
| NC_000023.10:g.135741424C>G , CM000685.1:g.135741424C>G | GRCh37 |
| NC_000023.9:g.135569090C>G | NCBI36 |
| NG_007280.1:g.16089C>G , LRG_141:g.16089C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695724.1:c.*254C>G | ENSP00000512122.1:n.*254C>G | |
| ENST00000695725.1:c.*191C>G | ENSP00000512123.1:n.*191C>G | |
| ENST00000695726.1:n.2604C>G | ||
| ENST00000695729.1:n.3439C>G | ||
| ENST00000370629.7:c.636C>G MANE Select | ENSP00000359663.2:p.His212Gln | |
| ENST00000370628.2:c.573C>G | ENSP00000359662.2:p.His191Gln | |
| ENST00000370629.6:c.636C>G | ENSP00000359663.2:p.His212Gln | |
| NM_000074.2:c.636C>G , LRG_141t1:c.636C>G | NP_000065.1:p.His212Gln | |
| NM_000074.3:c.636C>G MANE Select | NP_000065.1:p.His212Gln |