Linked Data
ClinVar Variation Id:
1233834
ClinVar RCV Id:
RCV001619016
dbSNP Id:
rs1371330955
gnomAD v2:
19-4099450-G-A
gnomAD v3:
19-4099452-G-A
gnomAD v4:
19-4099452-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.4099452G>A , CM000681.2:g.4099452G>A | GRCh38 |
| NC_000019.9:g.4099450G>A , CM000681.1:g.4099450G>A | GRCh37 |
| NC_000019.8:g.4050450G>A | NCBI36 |
| NG_007996.1:g.29677C>T , LRG_750:g.29677C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000394867.9:n.1145-38C>T | ||
| ENST00000687128.1:n.1145-38C>T | ||
| ENST00000688002.1:n.962C>T | ||
| ENST00000689792.1:n.646-74C>T | ||
| ENST00000262948.10:c.706-38C>T MANE Select | ENSP00000262948.4:n.706-38C>T | |
| ENST00000262948.9:c.706-38C>T | ENSP00000262948.3:n.706-38C>T | |
| ENST00000394867.8:c.415-38C>T | ENSP00000378336.1:n.415-38C>T | |
| ENST00000593364.5:n.653-38C>T | ||
| ENST00000595715.1:n.483C>T | ||
| ENST00000597263.5:n.169+1567C>T | ||
| ENST00000599021.1:c.29+1567C>T | ||
| ENST00000600584.5:n.1228C>T | ||
| ENST00000601786.5:n.1007-38C>T | ||
| ENST00000602167.5:n.426-38C>T | ||
| NM_030662.3:c.706-38C>T , LRG_750t1:c.706-38C>T | NP_109587.1:n.706-38C>T | |
| XM_006722799.2:c.705+1567C>T | XP_006722862.1:n.705+1567C>T | |
| XM_011528133.1:c.136-38C>T | XP_011526435.1:n.136-38C>T | |
| XM_017026989.1:c.706-38C>T | XP_016882478.1:n.706-38C>T | |
| XM_017026990.1:c.705+1567C>T | XP_016882479.1:n.705+1567C>T | |
| XM_017026991.1:c.*278C>T | XP_016882480.1:n.*278C>T | |
| NM_030662.4:c.706-38C>T MANE Select | NP_109587.1:n.706-38C>T |