Linked Data
ClinVar Variation Id:
1910164
ClinVar RCV Id:
RCV002593062
dbSNP Id:
rs755745244
ExAC:
8:55538949 C / T
gnomAD v2:
8-55538949-C-T
gnomAD v3:
8-54626389-C-T
gnomAD v4:
8-54626389-C-T
COSMIC:
COSM2719175
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.54626389C>T , CM000670.2:g.54626389C>T | GRCh38 |
| NC_000008.10:g.55538949C>T , CM000670.1:g.55538949C>T | GRCh37 |
| NC_000008.9:g.55701502C>T | NCBI36 |
| NG_009840.1:g.15323C>T | |
| NG_009840.2:g.15323C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000220676.2:c.2507C>T MANE Select | ENSP00000220676.1:p.Pro836Leu | |
| ENST00000636932.1:c.787+4101C>T | ENSP00000489857.1:n.787+4101C>T | |
| ENST00000637698.1:c.787+4101C>T | ENSP00000490104.1:n.787+4101C>T | |
| ENST00000220676.1:c.2507C>T | ENSP00000220676.1:p.Pro836Leu | |
| NM_006269.1:c.2507C>T | NP_006260.1:p.Pro836Leu | |
| XM_017013721.1:c.2528C>T | XP_016869210.1:p.Pro843Leu | |
| XM_017013722.1:c.2507C>T | XP_016869211.1:p.Pro836Leu | |
| NM_001375654.1:c.787+4101C>T | NP_001362583.1:n.787+4101C>T | |
| NM_006269.2:c.2507C>T MANE Select | NP_006260.1:p.Pro836Leu |