Linked Data
MyVariant Identifiers:
chr17:g.39780438G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41624186G>A , CM000679.2:g.41624186G>A | GRCh38 |
| NC_000017.10:g.39780438G>A , CM000679.1:g.39780438G>A | GRCh37 |
| NC_000017.9:g.37033964G>A | NCBI36 |
| NG_008625.1:g.5445C>T | |
| NG_009090.2:g.167527C>T , LRG_401:g.167527C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311208.13:c.324C>T MANE Select | ENSP00000308452.8:p.Ala108= | |
| ENST00000311208.12:c.324C>T | ENSP00000308452.8:p.Ala108= | |
| ENST00000463128.5:c.-292C>T | ENSP00000468672.1:n.-292C>T | |
| ENST00000491673.1:n.390C>T | ||
| ENST00000493253.5:n.111C>T | ||
| ENST00000540235.5:c.75C>T | ENSP00000441751.2:p.Ala25= | |
| ENST00000577817.3:c.279C>T | ENSP00000467418.1:p.Ala93= | |
| NM_000422.2:c.324C>T | NP_000413.1:p.Ala108= | |
| NM_000422.3:c.324C>T MANE Select | NP_000413.1:p.Ala108= |