Linked Data
MyVariant Identifiers:
chr3:g.191093050C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.191375261C>A , CM000665.2:g.191375261C>A | GRCh38 |
| NC_000003.11:g.191093050C>A , CM000665.1:g.191093050C>A | GRCh37 |
| NC_000003.10:g.192575744C>A | NCBI36 |
| NG_008994.1:g.51177C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392455.9:c.648C>A MANE Select | ENSP00000376249.4:p.Pro216= | |
| ENST00000392456.4:c.449-4898C>A | ENSP00000376250.4:n.449-4898C>A | |
| ENST00000392455.7:c.449-4898C>A | ENSP00000376249.3:n.449-4898C>A | |
| ENST00000392456.3:c.648C>A | ENSP00000376250.3:p.Pro216= | |
| NM_174908.3:c.449-4898C>A | NP_777568.1:n.449-4898C>A | |
| NM_178335.2:c.648C>A | NP_848018.1:p.Pro216= | |
| XM_011512460.1:c.648C>A | XP_011510762.1:p.Pro216= | |
| NM_178335.3:c.648C>A MANE Select | NP_848018.1:p.Pro216= | |
| NM_174908.4:c.449-4898C>A | NP_777568.1:n.449-4898C>A |