Linked Data
ClinVar Variation Id:
1052437
ClinVar RCV Id:
RCV002242695
dbSNP Id:
rs1865621723
gnomAD v4:
11-112086957-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112086957G>A , CM000673.2:g.112086957G>A | GRCh38 |
| NC_000011.9:g.111957681G>A , CM000673.1:g.111957681G>A | GRCh37 |
| NC_000011.8:g.111462891G>A | NCBI36 |
| NG_012337.2:g.5111G>A | |
| NG_033145.1:g.4842C>T | |
| NG_012337.3:g.5111G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000530923.6:c.50G>A | ENSP00000432946.2:p.Arg17Gln | |
| ENST00000534010.2:c.50G>A | ENSP00000433202.2:p.Arg17Gln | |
| ENST00000375549.8:c.50G>A MANE Select | ENSP00000364699.3:p.Arg17Gln | |
| ENST00000528021.6:c.50G>A | ENSP00000432465.1:p.Arg17Gln | |
| ENST00000640554.1:c.50G>A | ENSP00000491141.1:p.Arg17Gln | |
| ENST00000375549.7:c.50G>A | ENSP00000364699.3:p.Arg17Gln | |
| ENST00000525291.5:c.50G>A | ENSP00000436669.1:p.Arg17Gln | |
| ENST00000525987.5:n.55G>A | ||
| ENST00000526592.5:c.50G>A | ENSP00000432005.1:p.Arg17Gln | |
| ENST00000528021.5:c.50G>A | ENSP00000432465.1:p.Arg17Gln | |
| ENST00000528048.5:c.50G>A | ENSP00000436217.1:p.Arg17Gln | |
| ENST00000528182.5:c.50G>A | ENSP00000435475.1:p.Arg17Gln | |
| ENST00000530923.5:c.40G>A | ||
| ENST00000531744.5:c.50G>A | ENSP00000456957.1:p.Arg17Gln | |
| ENST00000532699.1:c.50G>A | ENSP00000456434.1:p.Arg17Gln | |
| ENST00000614349.4:c.50G>A | ENSP00000480666.1:p.Arg17Gln | |
| NM_001276503.1:c.50G>A | NP_001263432.1:p.Arg17Gln | |
| NM_001276504.1:c.50G>A | NP_001263433.1:p.Arg17Gln | |
| NM_001276506.1:c.50G>A | NP_001263435.1:p.Arg17Gln | |
| NM_003002.3:c.50G>A | NP_002993.1:p.Arg17Gln | |
| NR_077060.1:n.134G>A | ||
| NM_003002.4:c.50G>A MANE Select | NP_002993.1:p.Arg17Gln | |
| NM_001276503.2:c.50G>A | NP_001263432.1:p.Arg17Gln | |
| NM_001276504.2:c.50G>A | NP_001263433.1:p.Arg17Gln | |
| NM_001276506.2:c.50G>A | NP_001263435.1:p.Arg17Gln | |
| NR_077060.2:n.85G>A |