Linked Data
gnomAD v4:
19-35849253-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.35849253T>C , CM000681.2:g.35849253T>C | GRCh38 |
| NC_000019.9:g.36340155T>C , CM000681.1:g.36340155T>C | GRCh37 |
| NC_000019.8:g.41031995T>C | NCBI36 |
| NG_013356.2:g.25035A>G , LRG_693:g.25035A>G | |
| NG_051206.1:g.2619T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378910.10:c.823A>G MANE Select | ENSP00000368190.4:p.Thr275Ala | |
| ENST00000353632.6:c.823A>G | ENSP00000343634.5:p.Thr275Ala | |
| ENST00000378910.9:c.823A>G | ENSP00000368190.4:p.Thr275Ala | |
| NM_004646.3:c.823A>G , LRG_693t1:c.823A>G | NP_004637.1:p.Thr275Ala | |
| NM_004646.4:c.823A>G MANE Select | NP_004637.1:p.Thr275Ala |