Linked Data
MyVariant Identifiers:
chr3:g.98304473A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.98585629A>G , CM000665.2:g.98585629A>G | GRCh38 |
| NC_000003.11:g.98304473A>G , CM000665.1:g.98304473A>G | GRCh37 |
| NC_000003.10:g.99787163A>G | NCBI36 |
| NG_015994.1:g.12983T>C | |
| NG_015994.2:g.12983T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647941.2:c.984T>C MANE Select | ENSP00000497326.1:p.Arg328= | |
| ENST00000264193.2:c.984T>C | ENSP00000264193.2:p.Arg328= | |
| ENST00000510489.1:n.234T>C | ||
| NM_000097.5:c.984T>C | NP_000088.3:p.Arg328= | |
| XM_005247125.3:c.984T>C | XP_005247182.1:p.Arg328= | |
| NM_000097.7:c.984T>C MANE Select | NP_000088.3:p.Arg328= | |
| XM_005247125.4:c.984T>C | XP_005247182.1:p.Arg328= | |
| XR_001740025.2:n.1155T>C | ||
| XR_001740026.1:n.1719T>C | ||
| XR_001740027.1:n.1259T>C | ||
| XR_001740028.1:n.1225T>C |