Linked Data
dbSNP Id:
rs770427889
ExAC:
11:67353575 G / A
gnomAD v2:
11-67353575-G-A
gnomAD v4:
11-67586104-G-A
MyVariant Identifiers:
chr11:g.67353575G>A (hg19)
chr11:g.67353575_67353576delinsAA (hg19)
chr11:g.67586104G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67586104G>A , CM000673.2:g.67586104G>A | GRCh38 |
| NC_000011.9:g.67353575G>A , CM000673.1:g.67353575G>A | GRCh37 |
| NC_000011.8:g.67110151G>A | NCBI36 |
| NG_012075.1:g.7510G>A , LRG_723:g.7510G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398603.6:c.337-285G>A | ENSP00000381604.1:n.337-285G>A | |
| ENST00000398606.10:c.337G>A MANE Select | ENSP00000381607.3:p.Glu113Lys | |
| ENST00000646888.1:c.*53G>A | ENSP00000494477.1:n.*53G>A | |
| ENST00000398603.5:c.337-285G>A | ENSP00000381604.1:n.337-285G>A | |
| ENST00000398606.7:c.337G>A | ENSP00000381607.3:p.Glu113Lys | |
| ENST00000467591.1:n.448G>A | ||
| ENST00000494593.1:n.1132G>A | ||
| ENST00000495996.1:c.1G>A | ENSP00000484686.1:p.Glu1Lys | |
| ENST00000498765.5:c.400G>A | ||
| NM_000852.3:c.337G>A , LRG_723t1:c.337G>A | NP_000843.1:p.Glu113Lys | |
| NM_000852.4:c.337G>A MANE Select | NP_000843.1:p.Glu113Lys |