Linked Data
MyVariant Identifiers:
chr8:g.1244369T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.1296109T>G , CM000670.2:g.1296109T>G | GRCh38 |
| NC_000008.10:g.1244369T>G , CM000670.1:g.1244369T>G | GRCh37 |
| NC_000008.9:g.1231776T>G | NCBI36 |
| NG_009409.2:g.563391T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000421627.7:c.103+37226T>G | ENSP00000400258.3:n.103+37226T>G | |
| ENST00000637795.2:c.106+37226T>G MANE Select | ENSP00000489774.1:n.106+37226T>G | |
| NR_111948.1:n.2974A>C | ||
| XM_011534761.1:c.-135+37226T>G | XP_011533063.1:n.-135+37226T>G | |
| XM_011534762.1:c.-135+37226T>G | XP_011533064.1:n.-135+37226T>G | |
| NM_001346810.1:c.106+37226T>G | NP_001333739.1:n.106+37226T>G | |
| NM_001346810.2:c.106+37226T>G MANE Select | NP_001333739.1:n.106+37226T>G |