Linked Data
gnomAD v4:
17-56594615-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.56594615A>C , CM000679.2:g.56594615A>C | GRCh38 |
| NC_000017.10:g.54671976A>C , CM000679.1:g.54671976A>C | GRCh37 |
| NC_000017.9:g.52026975A>C | NCBI36 |
| NG_011958.1:g.5917A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000332822.6:c.392A>C MANE Select | ENSP00000328181.4:p.Gln131Pro | |
| ENST00000332822.4:c.392A>C | ENSP00000328181.4:p.Gln131Pro | |
| NM_005450.4:c.392A>C | NP_005441.1:p.Gln131Pro | |
| NM_005450.6:c.392A>C MANE Select | NP_005441.1:p.Gln131Pro |