Linked Data
MyVariant Identifiers:
chr17:g.54672247G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.56594886G>A , CM000679.2:g.56594886G>A | GRCh38 |
| NC_000017.10:g.54672247G>A , CM000679.1:g.54672247G>A | GRCh37 |
| NC_000017.9:g.52027246G>A | NCBI36 |
| NG_011958.1:g.6188G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000332822.6:c.663G>A MANE Select | ENSP00000328181.4:p.Gln221= | |
| ENST00000332822.4:c.663G>A | ENSP00000328181.4:p.Gln221= | |
| NM_005450.4:c.663G>A | NP_005441.1:p.Gln221= | |
| NM_005450.6:c.663G>A MANE Select | NP_005441.1:p.Gln221= |