Linked Data
dbSNP Id:
rs370922996
ExAC:
15:90335813 C / T
gnomAD v2:
15-90335813-C-T
gnomAD v3:
15-89792582-C-T
gnomAD v4:
15-89792582-C-T
MyVariant Identifiers:
chr15:g.90335813C>T (hg19)
chr15:g.90335813_90335821delinsTGGTTAGCA (hg19)
chr15:g.89792582C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.89792582C>T , CM000677.2:g.89792582C>T | GRCh38 |
| NC_000015.9:g.90335813C>T , CM000677.1:g.90335813C>T | GRCh37 |
| NC_000015.8:g.88136817C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300060.7:c.2250-20G>A MANE Select | ENSP00000300060.6:n.2250-20G>A | |
| ENST00000559874.2:c.2250-20G>A | ENSP00000452934.2:n.2250-20G>A | |
| ENST00000560137.2:c.2250-20G>A | ENSP00000453413.2:n.2250-20G>A | |
| ENST00000679248.1:c.2250-20G>A | ENSP00000502886.1:n.2250-20G>A | |
| ENST00000300060.6:c.2250-20G>A | ENSP00000300060.6:n.2250-20G>A | |
| ENST00000558740.1:n.154-20G>A | ||
| NM_001150.2:c.2250-20G>A | NP_001141.2:n.2250-20G>A | |
| XM_005254892.3:c.2250-20G>A | XP_005254949.1:n.2250-20G>A | |
| XM_011521473.1:c.2250-20G>A | XP_011519775.1:n.2250-20G>A | |
| XM_005254892.4:c.2250-20G>A | XP_005254949.1:n.2250-20G>A | |
| NM_001150.3:c.2250-20G>A MANE Select | NP_001141.2:n.2250-20G>A | |
| NM_001381923.1:c.2250-20G>A | NP_001368852.1:n.2250-20G>A | |
| NM_001381924.1:c.2250-20G>A | NP_001368853.1:n.2250-20G>A |