Linked Data
ClinVar Variation Id:
2854085
ClinVar RCV Id:
RCV003688481
gnomAD v4:
11-6616800-G-T
MyVariant Identifiers:
chr11:g.6638031G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6616800G>T , CM000673.2:g.6616800G>T | GRCh38 |
| NC_000011.9:g.6638031G>T , CM000673.1:g.6638031G>T | GRCh37 |
| NC_000011.8:g.6594607G>T | NCBI36 |
| NG_008653.1:g.7662C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682424.1:c.633C>A | ENSP00000507321.1:p.Gly211= | |
| ENST00000299427.12:c.747C>A MANE Select | ENSP00000299427.6:p.Gly249= | |
| ENST00000436873.7:c.312+501C>A | ||
| ENST00000524788.2:n.1906C>A | ||
| ENST00000524903.2:n.2022C>A | ||
| ENST00000528807.2:n.403C>A | ||
| ENST00000530040.2:n.480-297C>A | ||
| ENST00000533371.6:c.18C>A | ENSP00000437066.1:p.Gly6= | |
| ENST00000642892.1:c.18C>A | ENSP00000494165.1:p.Gly6= | |
| ENST00000643439.1:c.*487C>A | ENSP00000495849.1:n.*487C>A | |
| ENST00000643479.1:n.776C>A | ||
| ENST00000643516.1:c.396-297C>A | ||
| ENST00000644151.1:n.2186C>A | ||
| ENST00000644218.1:c.747C>A | ENSP00000493574.1:p.Gly249= | |
| ENST00000644683.1:c.*200C>A | ENSP00000494085.1:n.*200C>A | |
| ENST00000644810.1:c.468C>A | ENSP00000495895.1:p.Gly156= | |
| ENST00000644831.1:n.923C>A | ||
| ENST00000644933.1:c.18C>A | ENSP00000496133.1:p.Gly6= | |
| ENST00000645020.1:n.2037C>A | ||
| ENST00000645285.1:c.18C>A | ENSP00000495058.1:p.Gly6= | |
| ENST00000645331.1:n.1113C>A | ||
| ENST00000645620.1:c.18C>A | ENSP00000493657.1:p.Gly6= | |
| ENST00000646777.1:n.923C>A | ||
| ENST00000647016.1:n.1227C>A | ||
| ENST00000647152.1:c.18C>A | ENSP00000495893.1:p.Gly6= | |
| ENST00000647209.1:c.*616C>A | ENSP00000495558.1:n.*616C>A | |
| ENST00000647346.1:n.1767C>A | ||
| ENST00000299427.10:c.747C>A | ENSP00000299427.6:p.Gly249= | |
| ENST00000436873.6:c.451-297C>A | ENSP00000398136.2:n.451-297C>A | |
| ENST00000524788.1:n.447C>A | ||
| ENST00000528807.1:n.297C>A | ||
| ENST00000533371.5:c.18C>A | ENSP00000437066.1:p.Gly6= | |
| ENST00000611494.4:c.747C>A | ENSP00000484546.1:p.Gly249= | |
| NM_000391.3:c.747C>A | NP_000382.3:p.Gly249= | |
| NM_000391.4:c.747C>A MANE Select | NP_000382.3:p.Gly249= |