Linked Data
dbSNP Id:
rs139521261
ExAC:
8:144657653 C / T
gnomAD v2:
8-144657653-C-T
gnomAD v3:
8-143575483-C-T
gnomAD v4:
8-143575483-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.143575483C>T , CM000670.2:g.143575483C>T | GRCh38 |
| NC_000008.10:g.144657653C>T , CM000670.1:g.144657653C>T | GRCh37 |
| NC_000008.9:g.144728796C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000449291.7:c.1231G>A MANE Select | ENSP00000401508.2:p.Asp411Asn | |
| ENST00000340490.7:c.1231G>A | ENSP00000341136.3:p.Asp411Asn | |
| ENST00000426292.7:c.1231G>A | ENSP00000390949.3:p.Asp411Asn | |
| ENST00000435154.7:c.1231G>A | ENSP00000405670.3:p.Asp411Asn | |
| ENST00000449291.6:c.1231G>A | ENSP00000401508.2:p.Asp411Asn | |
| ENST00000460623.5:c.209G>A | ||
| ENST00000464332.5:n.775G>A | ||
| ENST00000525583.5:c.1015G>A | ||
| NM_001286829.1:c.1231G>A | NP_001273758.1:p.Asp411Asn | |
| NM_145201.5:c.1231G>A | NP_660202.3:p.Asp411Asn | |
| XM_011517377.1:c.1231G>A | XP_011515679.1:p.Asp411Asn | |
| NM_001363145.1:c.1150G>A | NP_001350074.1:p.Asp384Asn | |
| NM_001363146.1:c.547G>A | NP_001350075.1:p.Asp183Asn | |
| XM_017013975.2:c.1450G>A | XP_016869464.1:p.Asp484Asn | |
| XM_017013976.2:c.1450G>A | XP_016869465.1:p.Asp484Asn | |
| XM_017013977.2:c.1150G>A | XP_016869466.1:p.Asp384Asn | |
| XM_017013978.2:c.1450G>A | XP_016869467.1:p.Asp484Asn | |
| XM_017013979.2:c.547G>A | XP_016869468.1:p.Asp183Asn | |
| XM_024447332.1:c.868G>A | XP_024303100.1:p.Asp290Asn | |
| XM_024447333.1:c.466G>A | XP_024303101.1:p.Asp156Asn | |
| NM_145201.6:c.1231G>A MANE Select | NP_660202.3:p.Asp411Asn | |
| NM_001286829.2:c.1231G>A | NP_001273758.1:p.Asp411Asn |