Linked Data
dbSNP Id:
rs10420321
gnomAD v2:
19-10300417-A-G
gnomAD v3:
19-10189741-A-G
gnomAD v4:
19-10189741-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10189741A>G , CM000681.2:g.10189741A>G | GRCh38 |
| NC_000019.9:g.10300417A>G , CM000681.1:g.10300417A>G | GRCh37 |
| NC_000019.8:g.10161417A>G | NCBI36 |
| NG_028016.3:g.46546T>C , LRG_362:g.46546T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000359526.9:c.80+5079T>C MANE Select | ENSP00000352516.3:n.80+5079T>C | |
| ENST00000676610.1:c.80+5079T>C | ENSP00000504236.1:n.80+5079T>C | |
| ENST00000676820.1:n.136+5079T>C | ||
| ENST00000677013.1:c.80+5079T>C | ENSP00000503135.1:n.80+5079T>C | |
| ENST00000677250.1:c.80+5079T>C | ENSP00000502894.1:n.80+5079T>C | |
| ENST00000677634.1:c.80+5079T>C | ENSP00000504246.1:n.80+5079T>C | |
| ENST00000677685.1:c.80+5079T>C | ENSP00000503407.1:n.80+5079T>C | |
| ENST00000677946.1:c.80+5079T>C | ENSP00000504202.1:n.80+5079T>C | |
| ENST00000678804.1:c.80+5079T>C | ENSP00000503853.1:n.80+5079T>C | |
| ENST00000679103.1:c.80+5079T>C | ENSP00000503151.1:n.80+5079T>C | |
| ENST00000679313.1:c.80+5079T>C | ENSP00000504512.1:n.80+5079T>C | |
| ENST00000340748.8:c.80+5079T>C | ENSP00000345739.3:n.80+5079T>C | |
| ENST00000359526.8:c.80+5079T>C | ENSP00000352516.3:n.80+5079T>C | |
| ENST00000540357.5:c.-561+5202T>C | ENSP00000440457.2:n.-561+5202T>C | |
| ENST00000586800.5:c.-283-7664T>C | ENSP00000465555.1:n.-283-7664T>C | |
| ENST00000586988.5:c.80+5079T>C | ENSP00000464958.1:n.80+5079T>C | |
| ENST00000588118.5:c.245+5079T>C | ENSP00000465223.1:n.245+5079T>C | |
| ENST00000588952.5:c.-283-7664T>C | ENSP00000467050.1:n.-283-7664T>C | |
| ENST00000592054.5:c.-284+4792T>C | ENSP00000468359.1:n.-284+4792T>C | |
| ENST00000592342.5:c.-283-7664T>C | ENSP00000465993.1:n.-283-7664T>C | |
| ENST00000592705.5:c.80+5079T>C | ENSP00000466657.1:n.80+5079T>C | |
| NM_001130823.1:c.80+5079T>C , LRG_362t1:c.80+5079T>C | NP_001124295.1:n.80+5079T>C | |
| NM_001379.2:c.80+5079T>C | NP_001370.1:n.80+5079T>C | |
| XM_011527772.1:c.80+5079T>C | XP_011526074.1:n.80+5079T>C | |
| XM_011527773.1:c.80+5079T>C | XP_011526075.1:n.80+5079T>C | |
| XM_011527774.1:c.-284+4792T>C | XP_011526076.1:n.-284+4792T>C | |
| NM_001130823.2:c.80+5079T>C | NP_001124295.1:n.80+5079T>C | |
| NM_001318730.1:c.80+5079T>C | NP_001305659.1:n.80+5079T>C | |
| NM_001318731.1:c.-244+5079T>C | NP_001305660.1:n.-244+5079T>C | |
| NM_001379.3:c.80+5079T>C | NP_001370.1:n.80+5079T>C | |
| NM_001130823.3:c.80+5079T>C MANE Select | NP_001124295.1:n.80+5079T>C | |
| NM_001318730.2:c.80+5079T>C | NP_001305659.1:n.80+5079T>C | |
| NM_001318731.2:c.-244+5079T>C | NP_001305660.1:n.-244+5079T>C | |
| NM_001379.4:c.80+5079T>C | NP_001370.1:n.80+5079T>C |