Linked Data
MyVariant Identifiers:
chr6:g.1611097G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.1610862G>C , CM000668.2:g.1610862G>C | GRCh38 |
| NC_000006.11:g.1611097G>C , CM000668.1:g.1611097G>C | GRCh37 |
| NC_000006.10:g.1556096G>C | NCBI36 |
| NG_009368.1:g.5417G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000645831.2:c.417G>C MANE Select | ENSP00000493906.1:p.Val139= | |
| ENST00000380874.3:c.417G>C | ENSP00000370256.2:p.Val139= | |
| NM_001453.2:c.417G>C | NP_001444.2:p.Val139= | |
| NM_001453.3:c.417G>C MANE Select | NP_001444.2:p.Val139= |