Linked Data
ClinVar Variation Id:
213352
dbSNP Id:
rs368802769
ExAC:
5:127622512 C / T
gnomAD v2:
5-127622512-C-T
gnomAD v3:
5-128286820-C-T
gnomAD v4:
5-128286820-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128286820C>T , CM000667.2:g.128286820C>T | GRCh38 |
| NC_000005.9:g.127622512C>T , CM000667.1:g.127622512C>T | GRCh37 |
| NC_000005.8:g.127650411C>T | NCBI36 |
| NG_008750.1:g.256224G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703783.1:n.3694G>A | ||
| ENST00000262464.9:c.6910G>A MANE Select | ENSP00000262464.4:p.Asp2304Asn | |
| ENST00000262464.8:c.6910G>A | ENSP00000262464.4:p.Asp2304Asn | |
| ENST00000508053.5:c.6910G>A | ENSP00000424571.1:p.Asp2304Asn | |
| ENST00000619499.4:c.6907G>A | ENSP00000482132.1:p.Asp2303Asn | |
| NM_001999.3:c.6910G>A | NP_001990.2:p.Asp2304Asn | |
| XM_017009228.2:c.6757G>A | XP_016864717.1:p.Asp2253Asn | |
| NM_001999.4:c.6910G>A MANE Select | NP_001990.2:p.Asp2304Asn |