Linked Data
dbSNP Id:
rs1563338517
gnomAD v2:
7-131103401-G-T
gnomAD v3:
7-131418642-G-T
gnomAD v4:
7-131418642-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.131418642G>T , CM000669.2:g.131418642G>T | GRCh38 |
| NC_000007.13:g.131103401G>T , CM000669.1:g.131103401G>T | GRCh37 |
| NC_000007.12:g.130753941G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000352689.11:c.847+3932G>T MANE Select | ENSP00000323527.6:n.847+3932G>T | |
| ENST00000352689.10:c.847+3932G>T | ENSP00000323527.6:n.847+3932G>T | |
| ENST00000421797.6:c.571+3932G>T | ENSP00000398094.2:n.571+3932G>T | |
| ENST00000458153.5:c.*337+3932G>T | ENSP00000407705.1:n.*337+3932G>T | |
| ENST00000494785.5:n.864+3932G>T | ||
| NM_001145354.1:c.778+3932G>T | NP_001138826.1:n.778+3932G>T | |
| NM_013255.4:c.847+3932G>T | NP_037387.2:n.847+3932G>T | |
| XM_005250356.1:c.226+3932G>T | XP_005250413.1:n.226+3932G>T | |
| XM_006715993.1:c.847+3932G>T | XP_006716056.1:n.847+3932G>T | |
| XM_011516224.1:c.847+3932G>T | XP_011514526.1:n.847+3932G>T | |
| NM_001321316.1:c.226+3932G>T | NP_001308245.1:n.226+3932G>T | |
| XM_006715993.3:c.847+3932G>T | XP_006716056.1:n.847+3932G>T | |
| XM_011516224.3:c.847+3932G>T | XP_011514526.1:n.847+3932G>T | |
| XM_024446766.1:c.571+3932G>T | XP_024302534.1:n.571+3932G>T | |
| XM_024446767.1:c.571+3932G>T | XP_024302535.1:n.571+3932G>T | |
| NM_013255.5:c.847+3932G>T MANE Select | NP_037387.2:n.847+3932G>T | |
| NM_001145354.2:c.778+3932G>T | NP_001138826.1:n.778+3932G>T | |
| NM_001321316.2:c.226+3932G>T | NP_001308245.1:n.226+3932G>T |