Linked Data
dbSNP Id:
rs1379392149
gnomAD v2:
19-1399259-G-C
gnomAD v3:
19-1399260-G-C
gnomAD v4:
19-1399260-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1399260G>C , CM000681.2:g.1399260G>C | GRCh38 |
| NC_000019.9:g.1399259G>C , CM000681.1:g.1399259G>C | GRCh37 |
| NC_000019.8:g.1350259G>C | NCBI36 |
| NG_009785.1:g.7294C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252288.8:c.392-65C>G MANE Select | ENSP00000252288.1:n.392-65C>G | |
| ENST00000447102.8:c.392-65C>G | ENSP00000403536.2:n.392-65C>G | |
| ENST00000591788.3:c.75-65C>G | ||
| ENST00000640164.1:n.225-65C>G | ||
| ENST00000640762.1:c.323-65C>G | ENSP00000492031.1:n.323-65C>G | |
| ENST00000252288.6:c.392-65C>G | ENSP00000252288.1:n.392-65C>G | |
| ENST00000447102.7:c.392-65C>G | ENSP00000403536.2:n.392-65C>G | |
| ENST00000591788.2:c.77-65C>G | ENSP00000466341.2:n.77-65C>G | |
| NM_000156.5:c.392-65C>G | NP_000147.1:n.392-65C>G | |
| NM_138924.2:c.392-65C>G | NP_620279.1:n.392-65C>G | |
| NM_000156.6:c.392-65C>G MANE Select | NP_000147.1:n.392-65C>G | |
| NM_138924.3:c.392-65C>G | NP_620279.1:n.392-65C>G |