Linked Data
ClinVar Variation Id:
1079346
ClinVar RCV Id:
RCV001394618
dbSNP Id:
rs2144496522
gnomAD v4:
17-50168411-C-T
MyVariant Identifiers:
chr17:g.48245772C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.50168411C>T , CM000679.2:g.50168411C>T | GRCh38 |
| NC_000017.10:g.48245772C>T , CM000679.1:g.48245772C>T | GRCh37 |
| NC_000017.9:g.45600771C>T | NCBI36 |
| NG_008889.1:g.7407C>T , LRG_203:g.7407C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504073.2:c.423C>T | ENSP00000422030.2:p.Arg141= | |
| ENST00000511303.6:n.148C>T | ||
| ENST00000512526.2:c.414C>T | ENSP00000426606.2:n.414C>T | |
| ENST00000682109.1:c.303C>T | ENSP00000508041.1:p.Arg101= | |
| ENST00000683226.1:n.133C>T | ||
| ENST00000683294.1:c.423C>T | ENSP00000508134.1:p.Arg141= | |
| ENST00000262018.8:c.423C>T MANE Select | ENSP00000262018.3:p.Arg141= | |
| ENST00000262018.7:c.423C>T | ENSP00000262018.3:p.Arg141= | |
| ENST00000344627.10:c.423C>T | ENSP00000345522.6:p.Arg141= | |
| ENST00000502555.5:c.*82C>T | ENSP00000422817.1:n.*82C>T | |
| ENST00000511303.5:c.144C>T | ENSP00000426104.1:p.Arg48= | |
| ENST00000512526.1:c.258C>T | ||
| ENST00000513821.5:c.423C>T | ENSP00000426571.1:p.Arg141= | |
| ENST00000513942.5:n.214C>T | ||
| ENST00000514934.1:c.*129C>T | ENSP00000423168.1:n.*129C>T | |
| NM_000023.2:c.423C>T , LRG_203t1:c.423C>T | NP_000014.1:p.Arg141= | |
| NM_001135697.1:c.423C>T | NP_001129169.1:p.Arg141= | |
| XM_011525120.1:c.423C>T | XP_011523422.1:p.Arg141= | |
| XM_011525121.1:c.423C>T | XP_011523423.1:p.Arg141= | |
| XM_011525122.1:c.423C>T | XP_011523424.1:p.Arg141= | |
| XM_011525123.1:c.423C>T | XP_011523425.1:p.Arg141= | |
| XM_011525124.1:c.117C>T | XP_011523426.1:p.Arg39= | |
| XR_934517.1:n.489C>T | ||
| NM_000023.3:c.423C>T | NP_000014.1:p.Arg141= | |
| NM_001135697.2:c.423C>T | NP_001129169.1:p.Arg141= | |
| NR_135553.1:n.479C>T | ||
| XM_011525120.2:c.585C>T | XP_011523422.2:p.Arg195= | |
| XM_011525121.2:c.585C>T | XP_011523423.2:p.Arg195= | |
| XM_011525122.2:c.585C>T | XP_011523424.2:p.Arg195= | |
| XM_011525123.2:c.585C>T | XP_011523425.2:p.Arg195= | |
| XM_011525124.2:c.117C>T | XP_011523426.1:p.Arg39= | |
| XM_024450873.1:c.117C>T | XP_024306641.1:p.Arg39= | |
| XR_002958056.1:n.941C>T | ||
| NM_000023.4:c.423C>T MANE Select | NP_000014.1:p.Arg141= | |
| NM_001135697.3:c.423C>T | NP_001129169.1:p.Arg141= | |
| NR_135553.2:n.459C>T |