Linked Data
MyVariant Identifiers:
chr8:g.23069672T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.23212159T>G , CM000670.2:g.23212159T>G | GRCh38 |
| NC_000008.10:g.23069672T>G , CM000670.1:g.23069672T>G | GRCh37 |
| NC_000008.9:g.23125617T>G | NCBI36 |
| NG_032107.1:g.18009A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000221132.8:c.360A>C MANE Select | ENSP00000221132.3:p.Thr120= | |
| ENST00000221132.7:c.360A>C | ENSP00000221132.3:p.Thr120= | |
| ENST00000524158.5:c.-247A>C | ENSP00000428884.1:n.-247A>C | |
| ENST00000613472.1:c.32-9500A>C | ENSP00000480778.1:n.32-9500A>C | |
| NM_003844.3:c.360A>C | NP_003835.3:p.Thr120= | |
| NM_003844.4:c.360A>C MANE Select | NP_003835.3:p.Thr120= |