Linked Data
ClinVar Variation Id:
2971833
ClinVar RCV Id:
RCV003832895
MyVariant Identifiers:
chr17:g.63532638C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.65536520C>T , CM000679.2:g.65536520C>T | GRCh38 |
| NC_000017.10:g.63532638C>T , CM000679.1:g.63532638C>T | GRCh37 |
| NC_000017.9:g.60963100C>T | NCBI36 |
| NG_012142.1:g.30103G>A , LRG_296:g.30103G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307078.10:c.1941G>A MANE Select | ENSP00000302625.5:p.Glu647= | |
| ENST00000307078.9:c.1941G>A | ENSP00000302625.5:p.Glu647= | |
| ENST00000375702.5:c.1746G>A | ENSP00000364854.5:p.Glu582= | |
| ENST00000578251.1:n.163G>A | ||
| ENST00000611991.1:c.397-7820G>A | ENSP00000481191.1:n.397-7820G>A | |
| ENST00000618960.4:c.1746G>A | ENSP00000478916.1:p.Glu582= | |
| NM_004655.3:c.1941G>A , LRG_296t1:c.1941G>A | NP_004646.3:p.Glu647= | |
| XM_011525319.1:c.1941G>A | XP_011523621.1:p.Glu647= | |
| XM_011525320.1:c.1941G>A | XP_011523622.1:p.Glu647= | |
| XM_011525321.1:c.1941G>A | XP_011523623.1:p.Glu647= | |
| XM_011525322.1:c.1746G>A | XP_011523624.1:p.Glu582= | |
| NM_001363813.1:c.1746G>A | NP_001350742.1:p.Glu582= | |
| NM_004655.4:c.1941G>A MANE Select | NP_004646.3:p.Glu647= | |
| XM_011525319.2:c.1941G>A | XP_011523621.1:p.Glu647= | |
| XM_011525321.2:c.1941G>A | XP_011523623.1:p.Glu647= | |
| XM_017025192.1:c.1941G>A | XP_016880681.1:p.Glu647= | |
| XM_017025193.1:c.1746G>A | XP_016880682.1:p.Glu582= |