Linked Data
gnomAD v4:
3-81648972-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.81648972T>C , CM000665.2:g.81648972T>C | GRCh38 |
| NC_000003.11:g.81698123T>C , CM000665.1:g.81698123T>C | GRCh37 |
| NC_000003.10:g.81780813T>C | NCBI36 |
| NG_011810.1:g.117829A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000429644.7:c.575A>G MANE Select | ENSP00000410833.2:p.Lys192Arg | |
| ENST00000429644.6:c.575A>G | ENSP00000410833.2:p.Lys192Arg | |
| ENST00000486920.1:n.571A>G | ||
| ENST00000489715.1:c.452A>G | ENSP00000419638.1:p.Lys151Arg | |
| ENST00000498468.1:n.103A>G | ||
| NM_000158.3:c.575A>G | NP_000149.3:p.Lys192Arg | |
| NM_000158.4:c.575A>G MANE Select | NP_000149.4:p.Lys192Arg |