Linked Data
MyVariant Identifiers:
chr8:g.16850692T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.16993183T>C , CM000670.2:g.16993183T>C | GRCh38 |
| NC_000008.10:g.16850692T>C , CM000670.1:g.16850692T>C | GRCh37 |
| NC_000008.9:g.16895063T>C | NCBI36 |
| NG_015978.1:g.13983A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000180166.6:c.525A>G MANE Select | ENSP00000180166.5:p.Pro175= | |
| ENST00000180166.5:c.525A>G | ENSP00000180166.5:p.Pro175= | |
| ENST00000519941.1:c.229A>G | ||
| NM_019851.2:c.525A>G | NP_062825.1:p.Pro175= | |
| NM_019851.3:c.525A>G MANE Select | NP_062825.1:p.Pro175= |