Linked Data
dbSNP Id:
rs2089227178
gnomAD v3:
19-10115487-C-T
gnomAD v4:
19-10115487-C-T
MyVariant Identifiers:
chr19:g.10226163C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10115487C>T , CM000681.2:g.10115487C>T | GRCh38 |
| NC_000019.9:g.10226163C>T , CM000681.1:g.10226163C>T | GRCh37 |
| NC_000019.8:g.10087163C>T | NCBI36 |
| NG_047007.1:g.8967C>T | |
| NG_051197.1:g.9438G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253108.9:c.939G>A MANE Select | ENSP00000253108.3:p.Glu313= | |
| ENST00000253108.8:c.939G>A | ENSP00000253108.3:p.Glu313= | |
| ENST00000590158.1:n.958G>A | ||
| ENST00000593054.5:c.333G>A | ENSP00000467187.1:p.Glu111= | |
| NM_003755.3:c.939G>A | NP_003746.2:p.Glu313= | |
| NM_003755.4:c.939G>A | NP_003746.2:p.Glu313= | |
| NM_003755.5:c.939G>A MANE Select | NP_003746.2:p.Glu313= |