Linked Data
MyVariant Identifiers:
chr20:g.42747191A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.44118551A>G , CM000682.2:g.44118551A>G | GRCh38 |
| NC_000020.10:g.42747191A>G , CM000682.1:g.42747191A>G | GRCh37 |
| NC_000020.9:g.42180605A>G | NCBI36 |
| NG_031867.1:g.74028T>C , LRG_394:g.74028T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372980.4:c.1242T>C MANE Select | ENSP00000362071.3:p.Ile414= | |
| ENST00000372980.3:c.1242T>C | ENSP00000362071.3:p.Ile414= | |
| NM_020433.4:c.1242T>C , LRG_394t1:c.1242T>C | NP_065166.2:p.Ile414= | |
| XM_006723832.2:c.1242T>C | XP_006723895.1:p.Ile414= | |
| NM_020433.5:c.1242T>C MANE Select | NP_065166.2:p.Ile414= |