Linked Data
MyVariant Identifiers:
chr19:g.7591656T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7526770T>C , CM000681.2:g.7526770T>C | GRCh38 |
| NC_000019.9:g.7591656T>C , CM000681.1:g.7591656T>C | GRCh37 |
| NC_000019.8:g.7497656T>C | NCBI36 |
| NG_015806.1:g.9161T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000264079.11:c.415T>C MANE Select | ENSP00000264079.5:p.Leu139= | |
| ENST00000264079.10:c.415T>C | ENSP00000264079.5:p.Leu139= | |
| ENST00000394321.9:n.495T>C | ||
| ENST00000596008.1:n.377T>C | ||
| ENST00000598406.1:n.236T>C | ||
| ENST00000601003.1:c.415T>C | ENSP00000469074.1:p.Leu139= | |
| NM_020533.2:c.415T>C | NP_065394.1:p.Leu139= | |
| NM_020533.3:c.415T>C MANE Select | NP_065394.1:p.Leu139= |