Linked Data
MyVariant Identifiers:
chr3:g.191092942G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.191375153G>A , CM000665.2:g.191375153G>A | GRCh38 |
| NC_000003.11:g.191092942G>A , CM000665.1:g.191092942G>A | GRCh37 |
| NC_000003.10:g.192575636G>A | NCBI36 |
| NG_008994.1:g.51069G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392455.9:c.540G>A MANE Select | ENSP00000376249.4:p.Lys180= | |
| ENST00000392456.4:c.449-5006G>A | ENSP00000376250.4:n.449-5006G>A | |
| ENST00000392455.7:c.449-5006G>A | ENSP00000376249.3:n.449-5006G>A | |
| ENST00000392456.3:c.540G>A | ENSP00000376250.3:p.Lys180= | |
| NM_174908.3:c.449-5006G>A | NP_777568.1:n.449-5006G>A | |
| NM_178335.2:c.540G>A | NP_848018.1:p.Lys180= | |
| XM_011512460.1:c.540G>A | XP_011510762.1:p.Lys180= | |
| NM_178335.3:c.540G>A MANE Select | NP_848018.1:p.Lys180= | |
| NM_174908.4:c.449-5006G>A | NP_777568.1:n.449-5006G>A |