Linked Data
dbSNP Id:
rs920143041
gnomAD v3:
15-48445052-T-A
gnomAD v4:
15-48445052-T-A
MyVariant Identifiers:
chr15:g.48445052T>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48445052T>A , CM000677.2:g.48445052T>A | GRCh38 |
| NC_000015.9:g.48737249T>A , CM000677.1:g.48737249T>A | GRCh37 |
| NC_000015.8:g.46524541T>A | NCBI36 |
| NG_008805.2:g.205737A>T , LRG_778:g.205737A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.5917+324A>T | ENSP00000453958.2:n.5917+324A>T | |
| ENST00000674301.2:c.5917+324A>T | ENSP00000501333.2:n.5917+324A>T | |
| ENST00000684448.1:n.4591+324A>T | ||
| ENST00000316623.10:c.5917+324A>T MANE Select | ENSP00000325527.5:n.5917+324A>T | |
| ENST00000674301.1:c.916+324A>T | ENSP00000501333.1:n.916+324A>T | |
| ENST00000316623.9:c.5917+324A>T | ENSP00000325527.5:n.5917+324A>T | |
| ENST00000537463.6:c.*1680+324A>T | ENSP00000440294.2:n.*1680+324A>T | |
| ENST00000559133.5:c.1224+324A>T | ||
| ENST00000560820.1:n.37+324A>T | ||
| NM_000138.4:c.5917+324A>T , LRG_778t1:c.5917+324A>T | NP_000129.3:n.5917+324A>T | |
| NM_000138.5:c.5917+324A>T MANE Select | NP_000129.3:n.5917+324A>T |