Linked Data
dbSNP Id:
rs375333766
ExAC:
15:67358741 G / T
gnomAD v2:
15-67358741-G-T
gnomAD v3:
15-67066403-G-T
gnomAD v4:
15-67066403-G-T
MyVariant Identifiers:
chr15:g.67358741G>T (hg19)
chr15:g.67358741_67358742delinsTC (hg19)
chr15:g.67066403G>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.67066403G>T , CM000677.2:g.67066403G>T | GRCh38 |
| NC_000015.9:g.67358741G>T , CM000677.1:g.67358741G>T | GRCh37 |
| NC_000015.8:g.65145795G>T | NCBI36 |
| NG_011990.1:g.5547G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559460.6:c.-110+2459G>T | ENSP00000453082.2:n.-110+2459G>T | |
| ENST00000560424.2:c.206+43G>T | ENSP00000455540.2:n.206+43G>T | |
| ENST00000327367.9:c.206+43G>T MANE Select | ENSP00000332973.4:n.206+43G>T | |
| ENST00000327367.8:c.206+43G>T | ENSP00000332973.4:n.206+43G>T | |
| ENST00000559460.5:c.-110+2459G>T | ENSP00000453082.1:n.-110+2459G>T | |
| NM_005902.3:c.206+43G>T | NP_005893.1:n.206+43G>T | |
| XM_011521559.1:c.206+43G>T | XP_011519861.1:n.206+43G>T | |
| XM_011521559.3:c.206+43G>T | XP_011519861.1:n.206+43G>T | |
| NM_005902.4:c.206+43G>T MANE Select | NP_005893.1:n.206+43G>T |