Linked Data
MyVariant Identifiers:
chr4:g.187118748A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186197594A>G , CM000666.2:g.186197594A>G | GRCh38 |
| NC_000004.11:g.187118748A>G , CM000666.1:g.187118748A>G | GRCh37 |
| NC_000004.10:g.187355742A>G | NCBI36 |
| NG_007965.1:g.11075A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000378802.5:c.666A>G MANE Select | ENSP00000368079.4:p.Ala222= | |
| ENST00000378802.4:c.666A>G | ENSP00000368079.4:p.Ala222= | |
| ENST00000507209.5:n.1507A>G | ||
| NM_207352.3:c.666A>G | NP_997235.3:p.Ala222= | |
| XM_005262935.2:c.666A>G | XP_005262992.1:p.Ala222= | |
| XM_006714184.2:c.270A>G | XP_006714247.1:p.Ala90= | |
| XM_005262935.4:c.666A>G | XP_005262992.1:p.Ala222= | |
| XM_017008037.1:c.270A>G | XP_016863526.1:p.Ala90= | |
| NM_207352.4:c.666A>G MANE Select | NP_997235.3:p.Ala222= |