Linked Data
MyVariant Identifiers:
chr12:g.4481799T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4372633T>C , CM000674.2:g.4372633T>C | GRCh38 |
| NC_000012.11:g.4481799T>C , CM000674.1:g.4481799T>C | GRCh37 |
| NC_000012.10:g.4352060T>C | NCBI36 |
| NG_007087.1:g.12096A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000237837.2:c.276A>G MANE Select | ENSP00000237837.1:p.Arg92= | |
| ENST00000648100.1:c.*1967+6351T>C | ENSP00000497536.1:n.*1967+6351T>C | |
| ENST00000648269.1:n.1776A>G | ||
| ENST00000674624.1:c.*1204+6351T>C | ENSP00000501898.1:n.*1204+6351T>C | |
| ENST00000237837.1:c.276A>G | ENSP00000237837.1:p.Arg92= | |
| NM_020638.2:c.276A>G | NP_065689.1:p.Arg92= | |
| NM_020638.3:c.276A>G MANE Select | NP_065689.1:p.Arg92= |