Linked Data
ClinVar Variation Id:
2901543
ClinVar RCV Id:
RCV003601130
dbSNP Id:
rs1159236141
gnomAD v2:
17-7127942-C-T
gnomAD v3:
17-7224623-C-T
gnomAD v4:
17-7224623-C-T
MyVariant Identifiers:
chr17:g.7127942C>T (hg19)
chr17:g.7127942_7127948delinsTACCCCA (hg19)
chr17:g.7224623C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7224623C>T , CM000679.2:g.7224623C>T | GRCh38 |
| NC_000017.10:g.7127942C>T , CM000679.1:g.7127942C>T | GRCh37 |
| NC_000017.9:g.7068666C>T | NCBI36 |
| NG_007975.1:g.9790C>T | |
| NG_008391.2:g.428G>A | |
| NG_033038.1:g.14922G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356839.10:c.1679-19C>T MANE Select | ENSP00000349297.5:n.1679-19C>T | |
| ENST00000322910.9:c.*1634-19C>T | ENSP00000325395.5:n.*1634-19C>T | |
| ENST00000350303.9:c.1613-19C>T | ENSP00000344152.5:n.1613-19C>T | |
| ENST00000356839.9:c.1679-19C>T | ENSP00000349297.5:n.1679-19C>T | |
| ENST00000542255.6:c.536+71C>T | ||
| ENST00000543245.6:c.1748-19C>T | ENSP00000438689.2:n.1748-19C>T | |
| ENST00000578319.5:n.260-19C>T | ||
| ENST00000578711.1:n.1119C>T | ||
| ENST00000578809.5:n.251-19C>T | ||
| ENST00000579425.5:n.795-19C>T | ||
| ENST00000579546.1:c.414-19C>T | ||
| ENST00000582450.1:n.257C>T | ||
| ENST00000583074.5:n.299+71C>T | ||
| ENST00000583848.5:c.65-39C>T | ENSP00000466487.1:n.65-39C>T | |
| ENST00000583850.5:n.450-19C>T | ||
| ENST00000583858.5:c.610-19C>T | ||
| ENST00000585203.6:n.870-19C>T | ||
| NM_000018.3:c.1679-19C>T | NP_000009.1:n.1679-19C>T | |
| NM_001033859.2:c.1613-19C>T | NP_001029031.1:n.1613-19C>T | |
| NM_001270447.1:c.1748-19C>T | NP_001257376.1:n.1748-19C>T | |
| NM_001270448.1:c.1451-19C>T | NP_001257377.1:n.1451-19C>T | |
| XM_006721516.2:c.1678+71C>T | XP_006721579.2:n.1678+71C>T | |
| XM_011523829.1:c.1576+71C>T | XP_011522131.1:n.1576+71C>T | |
| XM_011523830.1:c.1577-19C>T | XP_011522132.1:n.1577-19C>T | |
| XR_934021.1:n.1782-19C>T | ||
| XR_934022.1:n.1688-19C>T | ||
| XR_934023.1:n.1687+71C>T | ||
| XM_006721516.3:c.1678+71C>T | XP_006721579.2:n.1678+71C>T | |
| XM_011523829.2:c.1576+71C>T | XP_011522131.1:n.1576+71C>T | |
| XM_011523830.2:c.1577-19C>T | XP_011522132.1:n.1577-19C>T | |
| XM_024450741.1:c.1667-19C>T | XP_024306509.1:n.1667-19C>T | |
| XR_934021.2:n.1734-19C>T | ||
| XR_934022.2:n.1640-19C>T | ||
| XR_934023.2:n.1639+71C>T | ||
| NM_000018.4:c.1679-19C>T MANE Select | NP_000009.1:n.1679-19C>T | |
| NM_001033859.3:c.1613-19C>T | NP_001029031.1:n.1613-19C>T | |
| NM_001270447.2:c.1748-19C>T | NP_001257376.1:n.1748-19C>T | |
| NM_001270448.2:c.1451-19C>T | NP_001257377.1:n.1451-19C>T |