Linked Data
dbSNP Id:
rs764928579
gnomAD v2:
6-32149382-C-G
gnomAD v3:
6-32181605-C-G
gnomAD v4:
6-32181605-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32181605C>G , CM000668.2:g.32181605C>G | GRCh38 |
| NC_000006.11:g.32149382C>G , CM000668.1:g.32149382C>G | GRCh37 |
| NC_000006.10:g.32257360C>G | NCBI36 |
| NG_029868.1:g.7718G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375076.9:c.991+1G>C MANE Select | ENSP00000364217.4:n.991+1G>C | |
| ENST00000375055.6:c.992G>C | ENSP00000364195.2:p.Gly331Ala | |
| ENST00000375065.6:c.178+1G>C | ENSP00000364206.6:n.178+1G>C | |
| ENST00000375067.7:c.836+1G>C | ENSP00000364208.3:n.836+1G>C | |
| ENST00000375069.7:c.1039+1G>C | ENSP00000364210.4:n.1039+1G>C | |
| ENST00000375070.7:c.662-128G>C | ENSP00000364211.4:n.662-128G>C | |
| ENST00000375076.8:c.991+1G>C | ENSP00000364217.4:n.991+1G>C | |
| ENST00000438221.6:c.1040G>C | ENSP00000387887.2:p.Gly347Ala | |
| ENST00000469940.5:n.31G>C | ||
| ENST00000473619.5:n.533+1G>C | ||
| ENST00000484849.5:n.1198+1G>C | ||
| ENST00000488669.5:n.534G>C | ||
| ENST00000620802.4:c.283-172G>C | ENSP00000484081.1:n.283-172G>C | |
| NM_001136.4:c.991+1G>C | NP_001127.1:n.991+1G>C | |
| NM_001206929.1:c.1039+1G>C | NP_001193858.1:n.1039+1G>C | |
| NM_001206932.1:c.949+1G>C | NP_001193861.1:n.949+1G>C | |
| NM_001206934.1:c.1040G>C | NP_001193863.1:p.Gly347Ala | |
| NM_001206936.1:c.940G>C | NP_001193865.1:p.Val314Leu | |
| NM_001206940.1:c.992G>C | NP_001193869.1:p.Gly331Ala | |
| NM_001206954.1:c.850G>C | NP_001193883.1:p.Val284Leu | |
| NM_001206966.1:c.992G>C | NP_001193895.1:p.Gly331Ala | |
| NM_172197.2:c.836+1G>C | NP_751947.1:n.836+1G>C | |
| NR_038190.1:n.1274+1G>C | ||
| XM_017010328.2:c.991G>C | XP_016865817.1:p.Val331Leu | |
| XR_001743189.2:n.1055+1G>C | ||
| XR_001743190.2:n.1007+1G>C | ||
| NM_001136.5:c.991+1G>C MANE Select | NP_001127.1:n.991+1G>C | |
| NM_001206932.2:c.949+1G>C | NP_001193861.1:n.949+1G>C | |
| NM_001206936.2:c.940G>C | NP_001193865.1:p.Val314Leu | |
| NM_001206940.2:c.992G>C | NP_001193869.1:p.Gly331Ala | |
| NM_001206954.2:c.850G>C | NP_001193883.1:p.Val284Leu | |
| NM_001206966.2:c.992G>C | NP_001193895.1:p.Gly331Ala | |
| NM_172197.3:c.836+1G>C | NP_751947.1:n.836+1G>C | |
| NR_038190.2:n.1205+1G>C | ||
| NM_001206929.2:c.1039+1G>C | NP_001193858.1:n.1039+1G>C | |
| NM_001206934.2:c.1040G>C | NP_001193863.1:p.Gly347Ala |