Linked Data
dbSNP Id:
rs746578005
ExAC:
4:68619783 T / G
gnomAD v2:
4-68619783-T-G
gnomAD v4:
4-67754065-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.67754065T>G , CM000666.2:g.67754065T>G | GRCh38 |
| NC_000004.11:g.68619783T>G , CM000666.1:g.68619783T>G | GRCh37 |
| NC_000004.10:g.68302378T>G | NCBI36 |
| NG_009293.1:g.7022A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000226413.5:c.271A>C MANE Select | ENSP00000226413.5:p.Thr91Pro | |
| ENST00000226413.4:c.271A>C | ENSP00000226413.4:p.Thr91Pro | |
| ENST00000420975.2:c.271A>C | ENSP00000397561.2:p.Thr91Pro | |
| NM_000406.2:c.271A>C | NP_000397.1:p.Thr91Pro | |
| NM_001012763.1:c.271A>C | NP_001012781.1:p.Thr91Pro | |
| NM_000406.3:c.271A>C MANE Select | NP_000397.1:p.Thr91Pro | |
| NM_001012763.2:c.271A>C | NP_001012781.1:p.Thr91Pro |