Linked Data
MyVariant Identifiers:
chr19:g.18898412C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18787603C>T , CM000681.2:g.18787603C>T | GRCh38 |
| NC_000019.9:g.18898412C>T , CM000681.1:g.18898412C>T | GRCh37 |
| NC_000019.8:g.18759412C>T | NCBI36 |
| NG_007070.1:g.8703G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222271.7:c.1023G>A MANE Select | ENSP00000222271.2:p.Glu341= | |
| ENST00000222271.6:c.1023G>A | ENSP00000222271.2:p.Glu341= | |
| ENST00000425807.1:c.864G>A | ENSP00000403792.1:p.Glu288= | |
| ENST00000542601.6:c.924G>A | ENSP00000439156.2:p.Glu308= | |
| NM_000095.2:c.1023G>A | NP_000086.2:p.Glu341= | |
| NM_000095.3:c.1023G>A MANE Select | NP_000086.2:p.Glu341= |