Linked Data
MyVariant Identifiers:
chr2:g.113832319T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.113074742T>A , CM000664.2:g.113074742T>A | GRCh38 |
| NC_000002.11:g.113832319T>A , CM000664.1:g.113832319T>A | GRCh37 |
| NC_000002.10:g.113548790T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000393197.3:c.138T>A | ENSP00000376893.2:p.Pro46= | |
| ENST00000341010.6:c.138T>A MANE Select | ENSP00000341794.2:p.Pro46= | |
| ENST00000393197.2:c.138T>A | ENSP00000376893.2:p.Pro46= | |
| ENST00000496265.1:n.204T>A | ||
| NM_032556.5:c.138T>A | NP_115945.4:p.Pro46= | |
| NM_173161.2:c.138T>A | NP_775184.1:p.Pro46= | |
| NM_032556.6:c.138T>A | NP_115945.4:p.Pro46= | |
| NM_173161.3:c.138T>A MANE Select | NP_775184.1:p.Pro46= |