Linked Data
MyVariant Identifiers:
chr5:g.174151776C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.174724773C>A , CM000667.2:g.174724773C>A | GRCh38 |
| NC_000005.9:g.174151776C>A , CM000667.1:g.174151776C>A | GRCh37 |
| NC_000005.8:g.174084382C>A | NCBI36 |
| NG_008124.1:g.5202C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000239243.7:c.114C>A MANE Select | ENSP00000239243.5:p.Arg38= | |
| ENST00000239243.6:c.114C>A | ENSP00000239243.5:p.Arg38= | |
| ENST00000507785.2:c.114C>A | ENSP00000427425.1:p.Arg38= | |
| NM_002449.4:c.114C>A | NP_002440.2:p.Arg38= | |
| NM_001363626.1:c.114C>A | NP_001350555.1:p.Arg38= | |
| NM_002449.5:c.114C>A MANE Select | NP_002440.2:p.Arg38= | |
| NM_001363626.2:c.114C>A | NP_001350555.1:p.Arg38= |