Linked Data
ClinVar Variation Id:
392407
ClinVar RCV Id:
RCV000437907
dbSNP Id:
rs1057524476
gnomAD v2:
5-147504327-G-A
gnomAD v3:
5-148124764-G-A
gnomAD v4:
5-148124764-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.148124764G>A , CM000667.2:g.148124764G>A | GRCh38 |
| NC_000005.9:g.147504327G>A , CM000667.1:g.147504327G>A | GRCh37 |
| NC_000005.8:g.147484520G>A | NCBI36 |
| NG_009633.1:g.65793G>A , LRG_110:g.65793G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000256084.8:c.2667-1G>A MANE Select | ENSP00000256084.7:n.2667-1G>A | |
| ENST00000256084.7:c.2667-1G>A | ENSP00000256084.7:n.2667-1G>A | |
| ENST00000359874.7:c.2667-1G>A | ENSP00000352936.3:n.2667-1G>A | |
| ENST00000398454.5:c.2667-1G>A | ENSP00000381472.1:n.2667-1G>A | |
| NM_001127698.1:c.2667-1G>A | NP_001121170.1:n.2667-1G>A | |
| NM_001127699.1:c.2667-1G>A | NP_001121171.1:n.2667-1G>A | |
| NM_006846.3:c.2667-1G>A , LRG_110t1:c.2667-1G>A | NP_006837.2:n.2667-1G>A | |
| XM_011537550.1:c.2610-1G>A | XP_011535852.1:n.2610-1G>A | |
| XM_011537551.1:c.2583-1G>A | XP_011535853.1:n.2583-1G>A | |
| XM_011537551.2:c.2583-1G>A | XP_011535853.1:n.2583-1G>A | |
| NM_001127698.2:c.2667-1G>A | NP_001121170.1:n.2667-1G>A | |
| NM_001127699.2:c.2667-1G>A | NP_001121171.1:n.2667-1G>A | |
| NM_006846.4:c.2667-1G>A MANE Select | NP_006837.2:n.2667-1G>A |