Linked Data
ClinVar Variation Id:
541779
dbSNP Id:
rs35732034
ExAC:
2:163124596 C / T
gnomAD v2:
2-163124596-C-T
gnomAD v3:
2-162268086-C-T
gnomAD v4:
2-162268086-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.162268086C>T , CM000664.2:g.162268086C>T | GRCh38 |
| NC_000002.11:g.163124596C>T , CM000664.1:g.163124596C>T | GRCh37 |
| NC_000002.10:g.162832842C>T | NCBI36 |
| NG_011495.1:g.55444G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000697291.1:c.*2404+1G>A | ENSP00000513228.1:n.*2404+1G>A | |
| ENST00000648433.1:c.2690+1G>A | ENSP00000496816.1:n.2690+1G>A | |
| ENST00000649426.1:n.52G>A | ||
| ENST00000649554.1:n.2417+1G>A | ||
| ENST00000649979.2:c.2807+1G>A MANE Select | ENSP00000497271.1:n.2807+1G>A | |
| ENST00000679938.1:c.2495+1G>A | ENSP00000505518.1:n.2495+1G>A | |
| ENST00000263642.2:c.2807+1G>A | ENSP00000263642.2:n.2807+1G>A | |
| NM_022168.3:c.2807+1G>A | NP_071451.2:n.2807+1G>A | |
| XM_011511628.1:c.2090+1G>A | XP_011509930.1:n.2090+1G>A | |
| NM_022168.4:c.2807+1G>A MANE Select | NP_071451.2:n.2807+1G>A |