Linked Data
dbSNP Id:
rs926769918
gnomAD v2:
3-38442258-G-T
gnomAD v3:
3-38400767-G-T
gnomAD v4:
3-38400767-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.38400767G>T , CM000665.2:g.38400767G>T | GRCh38 |
| NC_000003.11:g.38442258G>T , CM000665.1:g.38442258G>T | GRCh37 |
| NC_000003.10:g.38417262G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000207870.8:c.1439-124G>T MANE Select | ENSP00000207870.3:n.1439-124G>T | |
| ENST00000649234.1:c.*674-124G>T | ENSP00000497023.1:n.*674-124G>T | |
| ENST00000650590.1:c.1358-124G>T | ENSP00000496840.1:n.1358-124G>T | |
| ENST00000207870.7:c.1439-124G>T | ENSP00000207870.3:n.1439-124G>T | |
| ENST00000424034.5:c.*1102-124G>T | ENSP00000398845.1:n.*1102-124G>T | |
| ENST00000472721.1:n.316-124G>T | ||
| NM_005108.3:c.1439-124G>T | NP_005099.2:n.1439-124G>T | |
| XM_011534325.1:c.1439-124G>T | XP_011532627.1:n.1439-124G>T | |
| XM_011534326.1:c.1358-124G>T | XP_011532628.1:n.1358-124G>T | |
| XM_011534327.1:c.1439-124G>T | XP_011532629.1:n.1439-124G>T | |
| XM_011534328.1:c.1439-124G>T | XP_011532630.1:n.1439-124G>T | |
| XM_011534329.1:c.1439-124G>T | XP_011532631.1:n.1439-124G>T | |
| XM_011534330.1:c.1439-124G>T | XP_011532632.1:n.1439-124G>T | |
| NM_001349178.1:c.1439-124G>T | NP_001336107.1:n.1439-124G>T | |
| NM_001349179.1:c.1028-124G>T | NP_001336108.1:n.1028-124G>T | |
| NR_146068.1:n.1356-124G>T | ||
| XM_011534325.3:c.1439-124G>T | XP_011532627.1:n.1439-124G>T | |
| XM_011534327.2:c.1439-124G>T | XP_011532629.1:n.1439-124G>T | |
| XM_011534328.3:c.1439-124G>T | XP_011532630.1:n.1439-124G>T | |
| XM_011534329.2:c.1439-124G>T | XP_011532631.1:n.1439-124G>T | |
| XM_011534330.3:c.1439-124G>T | XP_011532632.1:n.1439-124G>T | |
| XM_017007595.1:c.1028-124G>T | XP_016863084.1:n.1028-124G>T | |
| XM_017007596.1:c.1241-124G>T | XP_016863085.1:n.1241-124G>T | |
| XM_017007597.1:c.758-124G>T | XP_016863086.1:n.758-124G>T | |
| XM_017007599.2:c.*49-124G>T | XP_016863088.1:n.*49-124G>T | |
| XM_024453850.1:c.1241-124G>T | XP_024309618.1:n.1241-124G>T | |
| NM_001349178.2:c.1439-124G>T | NP_001336107.1:n.1439-124G>T | |
| NM_005108.4:c.1439-124G>T MANE Select | NP_005099.2:n.1439-124G>T | |
| NR_146068.2:n.1331-124G>T | ||
| NM_001349179.2:c.1028-124G>T | NP_001336108.1:n.1028-124G>T |