Linked Data
MyVariant Identifiers:
chr16:g.17228488A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.17134631A>T , CM000678.2:g.17134631A>T | GRCh38 |
| NC_000016.9:g.17228488A>T , CM000678.1:g.17228488A>T | GRCh37 |
| NC_000016.8:g.17135989A>T | NCBI36 |
| NG_015843.1:g.341251T>A | |
| NG_015843.2:g.341251T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261381.7:c.1869T>A MANE Select | ENSP00000261381.6:p.Gly623= | |
| ENST00000261381.6:c.1869T>A | ENSP00000261381.6:p.Gly623= | |
| NM_022166.3:c.1869T>A | NP_071449.1:p.Gly623= | |
| XM_011522574.1:c.1869T>A | XP_011520876.1:p.Gly623= | |
| XR_933140.1:n.82+81A>T | ||
| XR_933141.1:n.75+81A>T | ||
| XR_933143.1:n.82+81A>T | ||
| NR_135179.1:n.47+81A>T | ||
| XM_017023539.2:c.1869T>A | XP_016879028.1:p.Gly623= | |
| XM_017023540.2:c.1869T>A | XP_016879029.1:p.Gly623= | |
| NM_022166.4:c.1869T>A MANE Select | NP_071449.1:p.Gly623= |