Linked Data
ClinVar Variation Id:
351620
dbSNP Id:
rs75086059
gnomAD v2:
5-148367238-G-A
gnomAD v3:
5-148987675-G-A
gnomAD v4:
5-148987675-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.148987675G>A , CM000667.2:g.148987675G>A | GRCh38 |
| NC_000005.9:g.148367238G>A , CM000667.1:g.148367238G>A | GRCh37 |
| NC_000005.8:g.148347431G>A | NCBI36 |
| NG_007947.2:g.80500C>T , LRG_269:g.80500C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000515425.6:c.*17036C>T MANE Select | ENSP00000423660.1:n.*17036C>T | |
| ENST00000504690.5:c.*12+16051C>T | ENSP00000425627.1:n.*12+16051C>T | |
| ENST00000510350.1:n.231+19206C>T | ||
| NM_024577.3:c.*17036C>T , LRG_269t1:c.*17036C>T | NP_078853.2:n.*17036C>T | |
| NM_024577.4:c.*17036C>T MANE Select | NP_078853.2:n.*17036C>T |