Linked Data
MyVariant Identifiers:
chr5:g.135382067A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.136046378A>C , CM000667.2:g.136046378A>C | GRCh38 |
| NC_000005.9:g.135382067A>C , CM000667.1:g.135382067A>C | GRCh37 |
| NC_000005.8:g.135409966A>C | NCBI36 |
| NG_012646.1:g.22484A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000442011.7:c.342A>C MANE Select | ENSP00000416330.2:p.Gly114= | |
| ENST00000442011.6:c.342A>C | ENSP00000416330.2:p.Gly114= | |
| ENST00000504185.5:n.499A>C | ||
| ENST00000506699.5:n.407A>C | ||
| ENST00000507018.5:c.259A>C | ||
| ENST00000515433.1:n.634A>C | ||
| NM_000358.2:c.342A>C | NP_000349.1:p.Gly114= | |
| NM_000358.3:c.342A>C MANE Select | NP_000349.1:p.Gly114= |