Linked Data
MyVariant Identifiers:
chr17:g.39768518G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41612266G>T , CM000679.2:g.41612266G>T | GRCh38 |
| NC_000017.10:g.39768518G>T , CM000679.1:g.39768518G>T | GRCh37 |
| NC_000017.9:g.37022044G>T | NCBI36 |
| NG_008301.1:g.5562C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301653.9:c.423C>A MANE Select | ENSP00000301653.3:p.Ala141= | |
| ENST00000301653.8:c.423C>A | ENSP00000301653.3:p.Ala141= | |
| ENST00000588319.1:n.500C>A | ||
| ENST00000593067.1:c.-292C>A | ENSP00000467124.1:n.-292C>A | |
| NM_005557.3:c.423C>A | NP_005548.2:p.Ala141= | |
| NM_005557.4:c.423C>A MANE Select | NP_005548.2:p.Ala141= |