Linked Data
dbSNP Id:
rs145489027
gnomAD v2:
4-21391194-G-A
gnomAD v3:
4-21389571-G-A
gnomAD v4:
4-21389571-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.21389571G>A , CM000666.2:g.21389571G>A | GRCh38 |
| NC_000004.11:g.21391194G>A , CM000666.1:g.21391194G>A | GRCh37 |
| NC_000004.10:g.21000292G>A | NCBI36 |
| NG_052969.1:g.564181C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000382152.7:c.62-506862C>T MANE Select | ENSP00000371587.2:n.62-506862C>T | |
| ENST00000382148.7:c.88+307779C>T | ENSP00000371583.3:n.88+307779C>T | |
| ENST00000382152.6:c.62-506862C>T | ENSP00000371587.2:n.62-506862C>T | |
| ENST00000447367.6:c.62-538904C>T | ENSP00000399080.2:n.62-538904C>T | |
| ENST00000509207.1:c.-24+154819C>T | ENSP00000423257.1:n.-24+154819C>T | |
| ENST00000515786.2:c.173+373350C>T | ENSP00000445321.1:n.173+373350C>T | |
| NM_001035003.1:c.88+307779C>T | NP_001030175.1:n.88+307779C>T | |
| NM_001035004.1:c.-24+154819C>T | NP_001030176.1:n.-24+154819C>T | |
| NM_025221.5:c.62-506862C>T | NP_079497.2:n.62-506862C>T | |
| NM_147181.3:c.62-538904C>T | NP_671710.1:n.62-538904C>T | |
| NM_147182.3:c.-24+373350C>T | NP_671711.1:n.-24+373350C>T | |
| XM_011513882.1:c.62-506862C>T | XP_011512184.1:n.62-506862C>T | |
| XM_011513885.1:c.88+307779C>T | XP_011512187.1:n.88+307779C>T | |
| XM_011513886.1:c.62-538904C>T | XP_011512188.1:n.62-538904C>T | |
| XM_011513887.1:c.-24+154819C>T | XP_011512189.1:n.-24+154819C>T | |
| XM_011513888.1:c.-24+373350C>T | XP_011512190.1:n.-24+373350C>T | |
| XM_011513885.3:c.88+307779C>T | XP_011512187.1:n.88+307779C>T | |
| XM_011513887.2:c.-24+154819C>T | XP_011512189.1:n.-24+154819C>T | |
| NM_025221.6:c.62-506862C>T MANE Select | NP_079497.2:n.62-506862C>T | |
| NM_001035003.2:c.88+307779C>T | NP_001030175.1:n.88+307779C>T | |
| NM_001035004.2:c.-24+154819C>T | NP_001030176.1:n.-24+154819C>T | |
| NM_147181.4:c.62-538904C>T | NP_671710.1:n.62-538904C>T | |
| NM_147182.4:c.-24+373350C>T | NP_671711.1:n.-24+373350C>T |