Linked Data
MyVariant Identifiers:
chr4:g.46125898A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.46123881A>G , CM000666.2:g.46123881A>G | GRCh38 |
| NC_000004.11:g.46125898A>G , CM000666.1:g.46125898A>G | GRCh37 |
| NC_000004.10:g.45820655A>G | NCBI36 |
| NG_046964.1:g.5185T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295452.5:c.33T>C MANE Select | ENSP00000295452.4:p.Pro11= | |
| ENST00000295452.4:c.33T>C | ENSP00000295452.4:p.Pro11= | |
| NM_173536.3:c.33T>C | NP_775807.2:p.Pro11= | |
| NM_173536.4:c.33T>C MANE Select | NP_775807.2:p.Pro11= |