Linked Data
MyVariant Identifiers:
chr4:g.187118223T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186197069T>A , CM000666.2:g.186197069T>A | GRCh38 |
| NC_000004.11:g.187118223T>A , CM000666.1:g.187118223T>A | GRCh37 |
| NC_000004.10:g.187355217T>A | NCBI36 |
| NG_007965.1:g.10550T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378802.5:c.543T>A MANE Select | ENSP00000368079.4:p.Ile181= | |
| ENST00000378802.4:c.543T>A | ENSP00000368079.4:p.Ile181= | |
| ENST00000507209.5:n.982T>A | ||
| NM_207352.3:c.543T>A | NP_997235.3:p.Ile181= | |
| XM_005262935.2:c.543T>A | XP_005262992.1:p.Ile181= | |
| XM_006714184.2:c.147T>A | XP_006714247.1:p.Ile49= | |
| XM_005262935.4:c.543T>A | XP_005262992.1:p.Ile181= | |
| XM_017008037.1:c.147T>A | XP_016863526.1:p.Ile49= | |
| NM_207352.4:c.543T>A MANE Select | NP_997235.3:p.Ile181= |