Linked Data
MyVariant Identifiers:
chr9:g.137726876G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.134835030G>A , CM000671.2:g.134835030G>A | GRCh38 |
| NC_000009.11:g.137726876G>A , CM000671.1:g.137726876G>A | GRCh37 |
| NC_000009.10:g.136866697G>A | NCBI36 |
| NG_008030.1:g.198225G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371820.4:c.5196G>A | ENSP00000360885.4:p.Arg1732= | |
| ENST00000371817.8:c.5196G>A MANE Select | ENSP00000360882.3:p.Arg1732= | |
| ENST00000371817.7:c.5196G>A | ENSP00000360882.3:p.Arg1732= | |
| ENST00000371820.3:c.454G>A | ||
| ENST00000618395.4:c.5196G>A | ENSP00000481360.1:p.Arg1732= | |
| NM_000093.4:c.5196G>A | NP_000084.3:p.Arg1732= | |
| NM_001278074.1:c.5196G>A | NP_001265003.1:p.Arg1732= | |
| NR_103451.2:n.71-14821C>T | ||
| XR_929712.1:n.5880G>A | ||
| XR_929713.1:n.5748G>A | ||
| NM_000093.5:c.5196G>A MANE Select | NP_000084.3:p.Arg1732= |