Linked Data
MyVariant Identifiers:
chr19:g.9325022C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.9214346C>T , CM000681.2:g.9214346C>T | GRCh38 |
| NC_000019.9:g.9325022C>T , CM000681.1:g.9325022C>T | GRCh37 |
| NC_000019.8:g.9186022C>T | NCBI36 |
| NG_027953.1:g.5526G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000641244.1:c.492G>A | ENSP00000493404.1:p.Lys164= | |
| ENST00000641669.1:c.492G>A MANE Select | ENSP00000493383.1:p.Lys164= | |
| ENST00000308682.3:c.492G>A | ENSP00000310488.2:p.Lys164= | |
| NM_001005191.2:c.492G>A | NP_001005191.1:p.Lys164= | |
| NM_001005191.3:c.492G>A MANE Select | NP_001005191.1:p.Lys164= |