Linked Data
MyVariant Identifiers:
chr19:g.46269870A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.45766612A>C , CM000681.2:g.45766612A>C | GRCh38 |
| NC_000019.9:g.46269870A>C , CM000681.1:g.46269870A>C | GRCh37 |
| NC_000019.8:g.50961710A>C | NCBI36 |
| NG_012745.1:g.7628T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000317578.7:c.1347T>G MANE Select | ENSP00000316842.4:p.Ala449= | |
| ENST00000317578.6:c.1347T>G | ENSP00000316842.4:p.Ala449= | |
| ENST00000560160.1:c.587-501T>G | ||
| ENST00000560168.1:c.*535T>G | ENSP00000453189.2:n.*535T>G | |
| ENST00000622857.1:c.16-650T>G | ENSP00000481365.1:n.16-650T>G | |
| NM_175875.4:c.1347T>G | NP_787071.2:p.Ala449= | |
| NM_175875.5:c.1347T>G MANE Select | NP_787071.3:p.Ala449= |