Linked Data
MyVariant Identifiers:
chr14:g.23890221A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23421012A>T , CM000676.2:g.23421012A>T | GRCh38 |
| NC_000014.8:g.23890221A>T , CM000676.1:g.23890221A>T | GRCh37 |
| NC_000014.7:g.22960061A>T | NCBI36 |
| NG_007884.1:g.19650T>A , LRG_384:g.19650T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355349.4:c.3282T>A MANE Select | ENSP00000347507.3:p.Ile1094= | |
| ENST00000355349.3:c.3282T>A | ENSP00000347507.3:p.Ile1094= | |
| NM_000257.3:c.3282T>A | NP_000248.2:p.Ile1094= | |
| XR_245686.3:n.3390T>A | ||
| XM_017021340.1:c.3282T>A | XP_016876829.1:p.Ile1094= | |
| NM_000257.4:c.3282T>A MANE Select | NP_000248.2:p.Ile1094= |