Linked Data
ClinVar Variation Id:
255869
dbSNP Id:
rs374790317
ExAC:
5:155756600 C / T
gnomAD v2:
5-155756600-C-T
gnomAD v3:
5-156329590-C-T
gnomAD v4:
5-156329590-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.156329590C>T , CM000667.2:g.156329590C>T | GRCh38 |
| NC_000005.9:g.155756600C>T , CM000667.1:g.155756600C>T | GRCh37 |
| NC_000005.8:g.155689178C>T | NCBI36 |
| NG_008693.2:g.464247C>T , LRG_205:g.464247C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000337851.9:c.3+11C>T MANE Select | ENSP00000338343.4:n.3+11C>T | |
| ENST00000337851.8:c.3+11C>T | ENSP00000338343.4:n.3+11C>T | |
| ENST00000435422.7:c.-1+2358C>T | ENSP00000403003.2:n.-1+2358C>T | |
| ENST00000517913.5:c.3+11C>T | ENSP00000429378.1:n.3+11C>T | |
| ENST00000524347.2:c.3+11C>T | ENSP00000430794.1:n.3+11C>T | |
| NM_000337.5:c.3+11C>T , LRG_205t1:c.3+11C>T | NP_000328.2:n.3+11C>T | |
| NM_001128209.1:c.-1+2358C>T | NP_001121681.1:n.-1+2358C>T | |
| NM_172244.2:c.3+11C>T | NP_758447.1:n.3+11C>T | |
| XM_005265966.3:c.3+11C>T | XP_005266023.1:n.3+11C>T | |
| XM_005265967.1:c.3+11C>T | XP_005266024.1:n.3+11C>T | |
| XM_006714911.2:c.3+11C>T | XP_006714974.1:n.3+11C>T | |
| XM_011534621.1:c.1-14899C>T | XP_011532923.1:n.1-14899C>T | |
| XR_941123.1:n.254+17863G>A | ||
| XM_005265966.5:c.3+11C>T | XP_005266023.1:n.3+11C>T | |
| XM_005265967.2:c.3+11C>T | XP_005266024.1:n.3+11C>T | |
| XM_011534621.2:c.1-14899C>T | XP_011532923.1:n.1-14899C>T | |
| XM_017009723.2:c.3+11C>T | XP_016865212.1:n.3+11C>T | |
| XM_017009724.1:c.3+11C>T | XP_016865213.1:n.3+11C>T | |
| NM_001128209.2:c.-1+2358C>T | NP_001121681.1:n.-1+2358C>T | |
| NM_172244.3:c.3+11C>T | NP_758447.1:n.3+11C>T | |
| NM_000337.6:c.3+11C>T MANE Select | NP_000328.2:n.3+11C>T |