Linked Data
dbSNP Id:
rs769758390
gnomAD v2:
19-18266917-G-C
gnomAD v3:
19-18156107-G-C
gnomAD v4:
19-18156107-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18156107G>C , CM000681.2:g.18156107G>C | GRCh38 |
| NC_000019.9:g.18266917G>C , CM000681.1:g.18266917G>C | GRCh37 |
| NC_000019.8:g.18127917G>C | NCBI36 |
| NG_033010.1:g.7930G>C | |
| NG_033010.2:g.7930G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222254.13:c.228G>C MANE Select | ENSP00000222254.6:p.Glu76Asp | |
| ENST00000617130.5:c.228G>C | ENSP00000477864.2:p.Glu76Asp | |
| ENST00000617642.2:c.228G>C | ENSP00000484714.2:p.Glu76Asp | |
| ENST00000222254.12:c.228G>C | ENSP00000222254.6:p.Glu76Asp | |
| ENST00000426902.5:c.228G>C | ENSP00000395636.1:p.Glu76Asp | |
| ENST00000593731.1:c.228G>C | ENSP00000471914.1:p.Glu76Asp | |
| ENST00000617130.4:c.228G>C | ENSP00000477864.1:p.Glu76Asp | |
| ENST00000617642.1:c.228G>C | ENSP00000484714.1:p.Glu76Asp | |
| NM_005027.3:c.228G>C | NP_005018.1:p.Glu76Asp | |
| NR_073517.1:n.768G>C | ||
| NM_005027.4:c.228G>C MANE Select | NP_005018.2:p.Glu76Asp | |
| NR_073517.2:n.783G>C | ||
| NR_162071.1:n.783G>C |