Linked Data
MyVariant Identifiers:
chr17:g.39780398T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41624146T>G , CM000679.2:g.41624146T>G | GRCh38 |
| NC_000017.10:g.39780398T>G , CM000679.1:g.39780398T>G | GRCh37 |
| NC_000017.9:g.37033924T>G | NCBI36 |
| NG_008625.1:g.5485A>C | |
| NG_009090.2:g.167567A>C , LRG_401:g.167567A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311208.13:c.364A>C MANE Select | ENSP00000308452.8:p.Arg122= | |
| ENST00000311208.12:c.364A>C | ENSP00000308452.8:p.Arg122= | |
| ENST00000463128.5:c.-252A>C | ENSP00000468672.1:n.-252A>C | |
| ENST00000491673.1:n.430A>C | ||
| ENST00000493253.5:n.151A>C | ||
| ENST00000540235.5:c.115A>C | ENSP00000441751.2:p.Arg39= | |
| ENST00000577817.3:c.319A>C | ENSP00000467418.1:p.Arg107= | |
| NM_000422.2:c.364A>C | NP_000413.1:p.Arg122= | |
| NM_000422.3:c.364A>C MANE Select | NP_000413.1:p.Arg122= |