Linked Data
ClinVar Variation Id:
352005
dbSNP Id:
rs199738915
ExAC:
5:149323938 C / T
gnomAD v2:
5-149323938-C-T
gnomAD v3:
5-149944375-C-T
gnomAD v4:
5-149944375-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149944375C>T , CM000667.2:g.149944375C>T | GRCh38 |
| NC_000005.9:g.149323938C>T , CM000667.1:g.149323938C>T | GRCh37 |
| NC_000005.8:g.149304131C>T | NCBI36 |
| NG_009102.1:g.5419G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000255266.10:c.299G>A MANE Select | ENSP00000255266.5:p.Arg100Gln | |
| ENST00000255266.9:c.299G>A | ENSP00000255266.5:p.Arg100Gln | |
| ENST00000508173.5:n.419G>A | ||
| ENST00000613228.1:c.299G>A | ENSP00000478060.1:p.Arg100Gln | |
| ENST00000617647.4:c.299G>A | ENSP00000482774.1:p.Arg100Gln | |
| NM_000440.2:c.299G>A | NP_000431.2:p.Arg100Gln | |
| XM_011537648.1:c.299G>A | XP_011535950.1:p.Arg100Gln | |
| XM_011537649.1:c.-72-9657G>A | XP_011535951.1:n.-72-9657G>A | |
| XM_017009572.2:c.299G>A | XP_016865061.1:p.Arg100Gln | |
| NM_000440.3:c.299G>A MANE Select | NP_000431.2:p.Arg100Gln |