Linked Data
dbSNP Id:
rs370892733
ExAC:
5:37060898 C / T
gnomAD v2:
5-37060898-C-T
gnomAD v3:
5-37060796-C-T
gnomAD v4:
5-37060796-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.37060796C>T , CM000667.2:g.37060796C>T | GRCh38 |
| NC_000005.9:g.37060898C>T , CM000667.1:g.37060898C>T | GRCh37 |
| NC_000005.8:g.37096655C>T | NCBI36 |
| NG_006987.1:g.188914C>T | |
| NG_006987.2:g.188914C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282516.13:c.7686-48C>T MANE Select | ENSP00000282516.8:n.7686-48C>T | |
| ENST00000652901.1:c.7539-48C>T | ENSP00000499536.1:n.7539-48C>T | |
| ENST00000282516.12:c.7686-48C>T | ENSP00000282516.8:n.7686-48C>T | |
| ENST00000448238.2:c.7686-48C>T | ENSP00000406266.2:n.7686-48C>T | |
| ENST00000513819.1:c.263+1631C>T | ENSP00000421504.1:n.263+1631C>T | |
| ENST00000514335.1:n.1568-48C>T | ||
| ENST00000621733.1:c.1-3782C>T | ENSP00000480694.1:n.1-3782C>T | |
| NM_015384.4:c.7686-48C>T | NP_056199.2:n.7686-48C>T | |
| NM_133433.3:c.7686-48C>T | NP_597677.2:n.7686-48C>T | |
| XM_005248280.2:c.7686-48C>T | XP_005248337.1:n.7686-48C>T | |
| XM_005248282.3:c.6942-48C>T | XP_005248339.2:n.6942-48C>T | |
| XM_006714467.2:c.7539-48C>T | XP_006714530.1:n.7539-48C>T | |
| XM_006714468.1:c.7488-48C>T | XP_006714531.1:n.7488-48C>T | |
| XM_011514014.1:c.7305-48C>T | XP_011512316.1:n.7305-48C>T | |
| XM_011514015.1:c.7264-48C>T | XP_011512317.1:n.7264-48C>T | |
| XM_005248280.3:c.7686-48C>T | XP_005248337.1:n.7686-48C>T | |
| XM_005248282.5:c.7026-48C>T | XP_005248339.3:n.7026-48C>T | |
| XM_006714468.2:c.7488-48C>T | XP_006714531.1:n.7488-48C>T | |
| XM_017009329.1:c.7539-48C>T | XP_016864818.1:n.7539-48C>T | |
| XM_017009330.2:c.6069-48C>T | XP_016864819.1:n.6069-48C>T | |
| XM_017009331.1:c.6060-48C>T | XP_016864820.1:n.6060-48C>T | |
| NM_133433.4:c.7686-48C>T MANE Select | NP_597677.2:n.7686-48C>T | |
| NM_015384.5:c.7686-48C>T | NP_056199.2:n.7686-48C>T |