Linked Data
ClinVar Variation Id:
476957
dbSNP Id:
rs144975214
ExAC:
19:40902030 G / A
gnomAD v2:
19-40902030-G-A
gnomAD v3:
19-40396123-G-A
gnomAD v4:
19-40396123-G-A
MyVariant Identifiers:
chr19:g.40902030G>A (hg19)
chr19:g.40902030_40902138delinsAGGGAGGTGCACATCGGGCACAGCCATCTCAGGCACCTTGGGGAGTTTTATCTCTGGGAGCTTCATGTCAGGGACTTTCATTTCACAGACTTTGGGCAGCTGCACCTCT (hg19)
chr19:g.40396123G>A (hg38)
chr19:g.40396123_40396231delinsAGGGAGGTGCACATCGGGCACAGCCATCTCAGGCACCTTGGGGAGTTTTATCTCTGGGAGCTTCATGTCAGGGACTTTCATTTCACAGACTTTGGGCAGCTGCACCTCT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.40396123G>A , CM000681.2:g.40396123G>A | GRCh38 |
| NC_000019.9:g.40902030G>A , CM000681.1:g.40902030G>A | GRCh37 |
| NC_000019.8:g.45593870G>A | NCBI36 |
| NG_007979.1:g.22242C>T , LRG_265:g.22242C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000324001.8:c.2229C>T MANE Select | ENSP00000326018.6:p.Pro743= | |
| ENST00000673881.1:c.1812C>T | ENSP00000501070.1:p.Pro604= | |
| ENST00000674005.2:c.2514C>T | ENSP00000501261.1:p.Pro838= | |
| ENST00000674773.1:c.1812C>T | ENSP00000502579.1:p.Pro604= | |
| ENST00000675517.1:c.2104C>T | ||
| ENST00000676076.1:c.2090C>T | ||
| ENST00000676260.1:c.2191C>T | ||
| ENST00000676316.1:c.2116C>T | ||
| ENST00000291825.11:c.*2434C>T | ENSP00000291825.6:n.*2434C>T | |
| ENST00000324001.7:c.2229C>T | ENSP00000326018.6:p.Pro743= | |
| NM_020956.2:c.*2434C>T , LRG_265t1:c.*2434C>T | NP_066007.1:n.*2434C>T | |
| NM_181882.2:c.2229C>T , LRG_265t2:c.2229C>T | NP_870998.2:p.Pro743= | |
| XM_011527171.1:c.2229C>T | XP_011525473.1:p.Pro743= | |
| XM_011527171.2:c.2229C>T | XP_011525473.1:p.Pro743= | |
| XM_017027046.1:c.2127C>T | XP_016882535.1:p.Pro709= | |
| XM_017027047.1:c.2127C>T | XP_016882536.1:p.Pro709= | |
| NM_181882.3:c.2229C>T MANE Select | NP_870998.2:p.Pro743= |