Linked Data
MyVariant Identifiers:
chr17:g.39768830T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41612578T>A , CM000679.2:g.41612578T>A | GRCh38 |
| NC_000017.10:g.39768830T>A , CM000679.1:g.39768830T>A | GRCh37 |
| NC_000017.9:g.37022356T>A | NCBI36 |
| NG_008301.1:g.5250A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301653.9:c.111A>T MANE Select | ENSP00000301653.3:p.Gly37= | |
| ENST00000301653.8:c.111A>T | ENSP00000301653.3:p.Gly37= | |
| ENST00000588319.1:n.188A>T | ||
| ENST00000590990.1:c.111A>T | ENSP00000467105.1:p.Gly37= | |
| ENST00000593067.1:c.-313+212A>T | ENSP00000467124.1:n.-313+212A>T | |
| NM_005557.3:c.111A>T | NP_005548.2:p.Gly37= | |
| NM_005557.4:c.111A>T MANE Select | NP_005548.2:p.Gly37= |