Linked Data
MyVariant Identifiers:
chr17:g.54671788G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.56594427G>A , CM000679.2:g.56594427G>A | GRCh38 |
| NC_000017.10:g.54671788G>A , CM000679.1:g.54671788G>A | GRCh37 |
| NC_000017.9:g.52026787G>A | NCBI36 |
| NG_011958.1:g.5729G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000332822.6:c.204G>A MANE Select | ENSP00000328181.4:p.Ser68= | |
| ENST00000332822.4:c.204G>A | ENSP00000328181.4:p.Ser68= | |
| NM_005450.4:c.204G>A | NP_005441.1:p.Ser68= | |
| NM_005450.6:c.204G>A MANE Select | NP_005441.1:p.Ser68= |