Linked Data
MyVariant Identifiers:
chr19:g.6714181C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6714170C>T , CM000681.2:g.6714170C>T | GRCh38 |
| NC_000019.9:g.6714181C>T , CM000681.1:g.6714181C>T | GRCh37 |
| NC_000019.8:g.6665181C>T | NCBI36 |
| NG_009557.1:g.11482G>A , LRG_27:g.11482G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.555G>A | ENSP00000512083.1:p.Glu185= | |
| ENST00000245907.11:c.678G>A MANE Select | ENSP00000245907.4:p.Glu226= | |
| ENST00000245907.10:c.678G>A | ENSP00000245907.4:p.Glu226= | |
| ENST00000595577.1:n.182G>A | ||
| NM_000064.3:c.678G>A | NP_000055.2:p.Glu226= | |
| NM_000064.4:c.678G>A MANE Select | NP_000055.2:p.Glu226= |