Linked Data
ClinVar Variation Id:
458745
dbSNP Id:
rs1297639505
gnomAD v3:
5-128357330-T-G
gnomAD v4:
5-128357330-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128357330T>G , CM000667.2:g.128357330T>G | GRCh38 |
| NC_000005.9:g.127693022T>G , CM000667.1:g.127693022T>G | GRCh37 |
| NC_000005.8:g.127720921T>G | NCBI36 |
| NG_008750.1:g.185714A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262464.9:c.2620A>C MANE Select | ENSP00000262464.4:p.Asn874His | |
| ENST00000262464.8:c.2620A>C | ENSP00000262464.4:p.Asn874His | |
| ENST00000508053.5:c.2620A>C | ENSP00000424571.1:p.Asn874His | |
| ENST00000508989.5:c.2521A>C | ENSP00000425596.1:p.Asn841His | |
| ENST00000619499.4:c.2617A>C | ENSP00000482132.1:p.Asn873His | |
| NM_001999.3:c.2620A>C | NP_001990.2:p.Asn874His | |
| XM_017009228.2:c.2467A>C | XP_016864717.1:p.Asn823His | |
| NM_001999.4:c.2620A>C MANE Select | NP_001990.2:p.Asn874His |