Linked Data
dbSNP Id:
rs746706897
ExAC:
3:39306999 A / G
gnomAD v2:
3-39306999-A-G
gnomAD v4:
3-39265508-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.39265508A>G , CM000665.2:g.39265508A>G | GRCh38 |
| NC_000003.11:g.39306999A>G , CM000665.1:g.39306999A>G | GRCh37 |
| NC_000003.10:g.39282003A>G | NCBI36 |
| NG_016362.1:g.21228T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000399220.3:c.1002T>C MANE Select | ENSP00000382166.3:p.His334= | |
| ENST00000358309.3:c.1098T>C | ENSP00000351059.3:p.His366= | |
| ENST00000399220.2:c.1002T>C | ENSP00000382166.2:p.His334= | |
| ENST00000541347.5:c.1002T>C | ENSP00000439140.1:p.His334= | |
| ENST00000542107.5:c.1002T>C | ENSP00000444928.1:p.His334= | |
| NM_001171171.1:c.1002T>C | NP_001164642.1:p.His334= | |
| NM_001171172.1:c.1002T>C | NP_001164643.1:p.His334= | |
| NM_001171174.1:c.1098T>C | NP_001164645.1:p.His366= | |
| NM_001337.3:c.1002T>C | NP_001328.1:p.His334= | |
| NM_001337.4:c.1002T>C MANE Select | NP_001328.1:p.His334= | |
| NM_001171171.2:c.1002T>C | NP_001164642.1:p.His334= | |
| NM_001171172.2:c.1002T>C | NP_001164643.1:p.His334= |