Linked Data
MyVariant Identifiers:
chr8:g.18257951G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.18400441G>C , CM000670.2:g.18400441G>C | GRCh38 |
| NC_000008.10:g.18257951G>C , CM000670.1:g.18257951G>C | GRCh37 |
| NC_000008.9:g.18302231G>C | NCBI36 |
| NG_012246.1:g.14197G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286479.4:c.438G>C MANE Select | ENSP00000286479.3:p.Val146= | |
| ENST00000286479.3:c.438G>C | ENSP00000286479.3:p.Val146= | |
| ENST00000520116.1:c.48G>C | ENSP00000428416.1:p.Val16= | |
| NM_000015.2:c.438G>C | NP_000006.2:p.Val146= | |
| XM_011544358.1:c.438G>C | XP_011542660.1:p.Val146= | |
| XM_017012938.1:c.438G>C | XP_016868427.1:p.Val146= | |
| NM_000015.3:c.438G>C MANE Select | NP_000006.2:p.Val146= |