Linked Data
dbSNP Id:
rs1439584609
gnomAD v2:
8-144657300-T-A
gnomAD v3:
8-143575130-T-A
gnomAD v4:
8-143575130-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.143575130T>A , CM000670.2:g.143575130T>A | GRCh38 |
| NC_000008.10:g.144657300T>A , CM000670.1:g.144657300T>A | GRCh37 |
| NC_000008.9:g.144728443T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000449291.7:c.1447-37A>T MANE Select | ENSP00000401508.2:n.1447-37A>T | |
| ENST00000340490.7:c.1447-37A>T | ENSP00000341136.3:n.1447-37A>T | |
| ENST00000426292.7:c.1408-37A>T | ENSP00000390949.3:n.1408-37A>T | |
| ENST00000435154.7:c.*34A>T | ENSP00000405670.3:n.*34A>T | |
| ENST00000449291.6:c.1447-37A>T | ENSP00000401508.2:n.1447-37A>T | |
| ENST00000460623.5:c.386-37A>T | ||
| ENST00000464332.5:n.991-37A>T | ||
| ENST00000498076.5:n.226-37A>T | ||
| ENST00000529179.1:n.194A>T | ||
| NM_001286829.1:c.1408-37A>T | NP_001273758.1:n.1408-37A>T | |
| NM_145201.5:c.1447-37A>T | NP_660202.3:n.1447-37A>T | |
| XM_011517377.1:c.1292-230A>T | XP_011515679.1:n.1292-230A>T | |
| NM_001363145.1:c.1366-37A>T | NP_001350074.1:n.1366-37A>T | |
| NM_001363146.1:c.763-37A>T | NP_001350075.1:n.763-37A>T | |
| XM_017013975.2:c.1666-37A>T | XP_016869464.1:n.1666-37A>T | |
| XM_017013976.2:c.1666-37A>T | XP_016869465.1:n.1666-37A>T | |
| XM_017013977.2:c.1366-37A>T | XP_016869466.1:n.1366-37A>T | |
| XM_017013978.2:c.1511-230A>T | XP_016869467.1:n.1511-230A>T | |
| XM_017013979.2:c.763-37A>T | XP_016869468.1:n.763-37A>T | |
| XM_024447332.1:c.929-230A>T | XP_024303100.1:n.929-230A>T | |
| XM_024447333.1:c.682-37A>T | XP_024303101.1:n.682-37A>T | |
| NM_145201.6:c.1447-37A>T MANE Select | NP_660202.3:n.1447-37A>T | |
| NM_001286829.2:c.1408-37A>T | NP_001273758.1:n.1408-37A>T |