Linked Data
MyVariant Identifiers:
chr9:g.80919768G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.78304852G>T , CM000671.2:g.78304852G>T | GRCh38 |
| NC_000009.11:g.80919768G>T , CM000671.1:g.80919768G>T | GRCh37 |
| NC_000009.10:g.80109588G>T | NCBI36 |
| NG_012165.1:g.12710G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376588.4:c.309G>T MANE Select | ENSP00000365773.3:p.Val103= | |
| ENST00000347159.6:c.309G>T | ENSP00000317606.2:p.Val103= | |
| ENST00000376588.3:c.309G>T | ENSP00000365773.3:p.Val103= | |
| NM_021154.4:c.309G>T | NP_066977.1:p.Val103= | |
| NM_058179.3:c.309G>T | NP_478059.1:p.Val103= | |
| NM_058179.4:c.309G>T MANE Select | NP_478059.1:p.Val103= | |
| NM_021154.5:c.309G>T | NP_066977.1:p.Val103= |