Linked Data
dbSNP Id:
rs1215030497
gnomAD v2:
17-73512748-G-T
gnomAD v3:
17-75516667-G-T
gnomAD v4:
17-75516667-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.75516667G>T , CM000679.2:g.75516667G>T | GRCh38 |
| NC_000017.10:g.73512748G>T , CM000679.1:g.73512748G>T | GRCh37 |
| NC_000017.9:g.71024343G>T | NCBI36 |
| NG_013041.1:g.5140G>T | |
| NG_033152.1:g.3917C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333213.11:c.56+51G>T MANE Select | ENSP00000327487.6:n.56+51G>T | |
| ENST00000434205.8:c.-83+281G>T | ENSP00000406559.4:n.-83+281G>T | |
| ENST00000545228.3:c.56+51G>T | ENSP00000438169.3:n.56+51G>T | |
| ENST00000579449.2:n.20+51G>T | ||
| ENST00000580013.6:n.65+51G>T | ||
| ENST00000583818.2:c.56+51G>T | ENSP00000461928.2:n.56+51G>T | |
| ENST00000679370.1:n.444-79G>T | ||
| ENST00000679429.1:c.56+51G>T | ENSP00000505403.1:n.56+51G>T | |
| ENST00000679782.1:c.56+51G>T | ENSP00000505995.1:n.56+51G>T | |
| ENST00000679928.1:c.56+51G>T | ENSP00000506071.1:n.56+51G>T | |
| ENST00000680528.1:n.81+51G>T | ||
| ENST00000680999.1:c.56+51G>T | ENSP00000504984.1:n.56+51G>T | |
| ENST00000681282.1:c.56+51G>T | ENSP00000506339.1:n.56+51G>T | |
| ENST00000333213.10:c.56+51G>T | ENSP00000327487.6:n.56+51G>T | |
| ENST00000434205.7:c.-83+281G>T | ENSP00000406559.3:n.-83+281G>T | |
| ENST00000580013.5:n.81+51G>T | ||
| ENST00000583173.5:c.56+51G>T | ENSP00000463619.1:n.56+51G>T | |
| ENST00000583454.1:n.91+51G>T | ||
| NM_207346.2:c.56+51G>T | NP_997229.2:n.56+51G>T | |
| XM_005257229.2:c.56+51G>T | XP_005257286.1:n.56+51G>T | |
| XM_006721821.2:c.-247-79G>T | XP_006721884.1:n.-247-79G>T | |
| XM_011524616.1:c.56+51G>T | XP_011522918.1:n.56+51G>T | |
| XM_011524617.1:c.56+51G>T | XP_011522919.1:n.56+51G>T | |
| XM_011524618.1:c.56+51G>T | XP_011522920.1:n.56+51G>T | |
| XR_243646.2:n.86+51G>T | ||
| XM_005257229.4:c.56+51G>T | XP_005257286.1:n.56+51G>T | |
| XR_243646.4:n.92+51G>T | ||
| NM_207346.3:c.56+51G>T MANE Select | NP_997229.2:n.56+51G>T |