Linked Data
dbSNP Id:
rs747238624
ExAC:
7:87229487 C / A
gnomAD v2:
7-87229487-C-A
gnomAD v3:
7-87600171-C-A
gnomAD v4:
7-87600171-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.87600171C>A , CM000669.2:g.87600171C>A | GRCh38 |
| NC_000007.13:g.87229487C>A , CM000669.1:g.87229487C>A | GRCh37 |
| NC_000007.12:g.87067423C>A | NCBI36 |
| NG_011513.1:g.118078G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265724.8:c.14G>T | ENSP00000265724.3:p.Gly5Val | |
| ENST00000622132.5:c.14G>T MANE Select | ENSP00000478255.1:p.Gly5Val | |
| ENST00000265724.7:c.14G>T | ENSP00000265724.3:p.Gly5Val | |
| ENST00000416177.1:c.14G>T | ENSP00000399419.1:p.Gly5Val | |
| ENST00000543898.5:c.14G>T | ENSP00000444095.1:p.Gly5Val | |
| ENST00000622132.4:c.14G>T | ENSP00000478255.1:p.Gly5Val | |
| NM_000927.4:c.14G>T | NP_000918.2:p.Gly5Val | |
| NM_001348944.1:c.14G>T | NP_001335873.1:p.Gly5Val | |
| NM_001348945.1:c.224G>T | NP_001335874.1:p.Gly75Val | |
| NM_001348946.1:c.14G>T | NP_001335875.1:p.Gly5Val | |
| NM_001348946.2:c.14G>T MANE Select | NP_001335875.1:p.Gly5Val | |
| NM_000927.5:c.14G>T | NP_000918.2:p.Gly5Val | |
| NM_001348944.2:c.14G>T | NP_001335873.1:p.Gly5Val | |
| NM_001348945.2:c.224G>T | NP_001335874.1:p.Gly75Val |