Linked Data
ClinVar Variation Id:
165227
ClinVar RCV Id:
RCV000151869
dbSNP Id:
rs369889635
gnomAD v3:
5-156329536-A-T
gnomAD v4:
5-156329536-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.156329536A>T , CM000667.2:g.156329536A>T | GRCh38 |
| NC_000005.9:g.155756546A>T , CM000667.1:g.155756546A>T | GRCh37 |
| NC_000005.8:g.155689124A>T | NCBI36 |
| NG_008693.2:g.464193A>T , LRG_205:g.464193A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000337851.9:c.-41A>T MANE Select | ENSP00000338343.4:n.-41A>T | |
| ENST00000337851.8:c.-41A>T | ENSP00000338343.4:n.-41A>T | |
| ENST00000435422.7:c.-1+2304A>T | ENSP00000403003.2:n.-1+2304A>T | |
| ENST00000517913.5:c.-41A>T | ENSP00000429378.1:n.-41A>T | |
| ENST00000524347.2:c.-41A>T | ENSP00000430794.1:n.-41A>T | |
| NM_000337.5:c.-41A>T , LRG_205t1:c.-41A>T | NP_000328.2:n.-41A>T | |
| NM_001128209.1:c.-1+2304A>T | NP_001121681.1:n.-1+2304A>T | |
| NM_172244.2:c.-41A>T | NP_758447.1:n.-41A>T | |
| XM_005265966.3:c.-41A>T | XP_005266023.1:n.-41A>T | |
| XM_005265967.1:c.-41A>T | XP_005266024.1:n.-41A>T | |
| XM_006714911.2:c.-41A>T | XP_006714974.1:n.-41A>T | |
| XM_011534621.1:c.1-14953A>T | XP_011532923.1:n.1-14953A>T | |
| XR_941123.1:n.254+17917T>A | ||
| XM_005265966.5:c.-41A>T | XP_005266023.1:n.-41A>T | |
| XM_005265967.2:c.-41A>T | XP_005266024.1:n.-41A>T | |
| XM_011534621.2:c.1-14953A>T | XP_011532923.1:n.1-14953A>T | |
| XM_017009723.2:c.-41A>T | XP_016865212.1:n.-41A>T | |
| XM_017009724.1:c.-41A>T | XP_016865213.1:n.-41A>T | |
| NM_001128209.2:c.-1+2304A>T | NP_001121681.1:n.-1+2304A>T | |
| NM_172244.3:c.-41A>T | NP_758447.1:n.-41A>T | |
| NM_000337.6:c.-41A>T MANE Select | NP_000328.2:n.-41A>T |