Linked Data
dbSNP Id:
rs753697440
gnomAD v2:
7-87150040-T-C
gnomAD v3:
7-87520724-T-C
gnomAD v4:
7-87520724-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.87520724T>C , CM000669.2:g.87520724T>C | GRCh38 |
| NC_000007.13:g.87150040T>C , CM000669.1:g.87150040T>C | GRCh37 |
| NC_000007.12:g.86987976T>C | NCBI36 |
| NG_011513.1:g.197525A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265724.8:c.2786+52A>G | ENSP00000265724.3:n.2786+52A>G | |
| ENST00000622132.5:c.2786+52A>G MANE Select | ENSP00000478255.1:n.2786+52A>G | |
| ENST00000265724.7:c.2786+52A>G | ENSP00000265724.3:n.2786+52A>G | |
| ENST00000483831.1:n.344+52A>G | ||
| ENST00000488737.6:n.428+52A>G | ||
| ENST00000496821.5:n.414+52A>G | ||
| ENST00000543898.5:c.2594+52A>G | ENSP00000444095.1:n.2594+52A>G | |
| ENST00000622132.4:c.2786+52A>G | ENSP00000478255.1:n.2786+52A>G | |
| NM_000927.4:c.2786+52A>G | NP_000918.2:n.2786+52A>G | |
| NM_001348944.1:c.2786+52A>G | NP_001335873.1:n.2786+52A>G | |
| NM_001348945.1:c.2996+52A>G | NP_001335874.1:n.2996+52A>G | |
| NM_001348946.1:c.2786+52A>G | NP_001335875.1:n.2786+52A>G | |
| NM_001348946.2:c.2786+52A>G MANE Select | NP_001335875.1:n.2786+52A>G | |
| NM_000927.5:c.2786+52A>G | NP_000918.2:n.2786+52A>G | |
| NM_001348944.2:c.2786+52A>G | NP_001335873.1:n.2786+52A>G | |
| NM_001348945.2:c.2996+52A>G | NP_001335874.1:n.2996+52A>G |