Linked Data
dbSNP Id:
rs17053082
gnomAD v2:
5-155394230-C-T
gnomAD v3:
5-155967220-C-T
gnomAD v4:
5-155967220-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.155967220C>T , CM000667.2:g.155967220C>T | GRCh38 |
| NC_000005.9:g.155394230C>T , CM000667.1:g.155394230C>T | GRCh37 |
| NC_000005.8:g.155326808C>T | NCBI36 |
| NG_008693.2:g.101877C>T , LRG_205:g.101877C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000517913.5:c.-282+96796C>T | ENSP00000429378.1:n.-282+96796C>T | |
| XM_017009723.2:c.-208+96796C>T | XP_016865212.1:n.-208+96796C>T | |
| XM_017009724.1:c.-207-156636C>T | XP_016865213.1:n.-207-156636C>T |