Linked Data
ClinVar Variation Id:
665948
dbSNP Id:
rs575262156
gnomAD v3:
11-112088940-G-A
gnomAD v4:
11-112088940-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112088940G>A , CM000673.2:g.112088940G>A | GRCh38 |
| NC_000011.9:g.111959664G>A , CM000673.1:g.111959664G>A | GRCh37 |
| NC_000011.8:g.111464874G>A | NCBI36 |
| NG_012337.2:g.7094G>A | |
| NG_033145.1:g.2859C>T | |
| NG_012337.3:g.7094G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000530923.6:c.243G>A | ENSP00000432946.2:p.Pro81= | |
| ENST00000534010.2:c.243G>A | ENSP00000433202.2:p.Pro81= | |
| ENST00000375549.8:c.243G>A MANE Select | ENSP00000364699.3:p.Pro81= | |
| ENST00000528021.6:c.243G>A | ENSP00000432465.1:p.Pro81= | |
| ENST00000640554.1:c.*315G>A | ENSP00000491141.1:n.*315G>A | |
| ENST00000375549.7:c.243G>A | ENSP00000364699.3:p.Pro81= | |
| ENST00000525291.5:c.126G>A | ENSP00000436669.1:p.Pro42= | |
| ENST00000525987.5:n.248G>A | ||
| ENST00000526592.5:c.243G>A | ENSP00000432005.1:p.Pro81= | |
| ENST00000528021.5:c.243G>A | ENSP00000432465.1:p.Pro81= | |
| ENST00000528048.5:c.169+967G>A | ENSP00000436217.1:n.169+967G>A | |
| ENST00000528182.5:c.243G>A | ENSP00000435475.1:p.Pro81= | |
| ENST00000530923.5:c.233G>A | ||
| ENST00000531744.5:c.243G>A | ENSP00000456957.1:p.Pro81= | |
| ENST00000532699.1:c.243G>A | ENSP00000456434.1:p.Pro81= | |
| ENST00000534010.1:c.74G>A | ||
| ENST00000614349.4:c.243G>A | ENSP00000480666.1:p.Pro81= | |
| NM_001276503.1:c.169+967G>A | NP_001263432.1:n.169+967G>A | |
| NM_001276504.1:c.126G>A | NP_001263433.1:p.Pro42= | |
| NM_001276506.1:c.243G>A | NP_001263435.1:p.Pro81= | |
| NM_003002.3:c.243G>A | NP_002993.1:p.Pro81= | |
| NR_077060.1:n.327G>A | ||
| NM_003002.4:c.243G>A MANE Select | NP_002993.1:p.Pro81= | |
| NM_001276503.2:c.169+967G>A | NP_001263432.1:n.169+967G>A | |
| NM_001276504.2:c.126G>A | NP_001263433.1:p.Pro42= | |
| NM_001276506.2:c.243G>A | NP_001263435.1:p.Pro81= | |
| NR_077060.2:n.278G>A |