Linked Data
dbSNP Id:
rs1429641363
gnomAD v2:
3-10191860-C-G
gnomAD v3:
3-10150176-C-G
gnomAD v4:
3-10150176-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10150176C>G , CM000665.2:g.10150176C>G | GRCh38 |
| NC_000003.11:g.10191860C>G , CM000665.1:g.10191860C>G | GRCh37 |
| NC_000003.10:g.10166860C>G | NCBI36 |
| NG_008212.3:g.13542C>G , LRG_322:g.13542C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000696142.1:c.*530C>G | ENSP00000512434.1:n.*530C>G | |
| ENST00000696143.1:c.989C>G | ENSP00000512435.1:n.989C>G | |
| ENST00000696153.1:c.*211C>G | ENSP00000512444.1:n.*211C>G | |
| ENST00000256474.3:c.*211C>G MANE Select | ENSP00000256474.3:n.*211C>G | |
| ENST00000256474.2:c.*211C>G | ENSP00000256474.2:n.*211C>G | |
| ENST00000345392.2:c.*211C>G | ENSP00000344757.2:n.*211C>G | |
| NM_000551.3:c.*211C>G , LRG_322t1:c.*211C>G | NP_000542.1:n.*211C>G | |
| NM_198156.2:c.*211C>G | NP_937799.1:n.*211C>G | |
| NM_001354723.1:c.*407C>G | NP_001341652.1:n.*407C>G | |
| NM_000551.4:c.*211C>G MANE Select | NP_000542.1:n.*211C>G | |
| NM_001354723.2:c.*407C>G | NP_001341652.1:n.*407C>G | |
| NM_198156.3:c.*211C>G | NP_937799.1:n.*211C>G |