Linked Data
dbSNP Id:
rs1226789179
gnomAD v2:
17-7123585-G-A
gnomAD v3:
17-7220266-G-A
gnomAD v4:
17-7220266-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7220266G>A , CM000679.2:g.7220266G>A | GRCh38 |
| NC_000017.10:g.7123585G>A , CM000679.1:g.7123585G>A | GRCh37 |
| NC_000017.9:g.7064309G>A | NCBI36 |
| NG_007975.1:g.5433G>A | |
| NG_008391.2:g.4785C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356839.10:c.138+69G>A MANE Select | ENSP00000349297.5:n.138+69G>A | |
| ENST00000322910.9:c.*93+69G>A | ENSP00000325395.5:n.*93+69G>A | |
| ENST00000350303.9:c.138+69G>A | ENSP00000344152.5:n.138+69G>A | |
| ENST00000356839.9:c.138+69G>A | ENSP00000349297.5:n.138+69G>A | |
| ENST00000543245.6:c.207+69G>A | ENSP00000438689.2:n.207+69G>A | |
| ENST00000577191.5:n.215+69G>A | ||
| ENST00000577433.5:n.75G>A | ||
| ENST00000577857.5:n.228+69G>A | ||
| ENST00000578269.5:n.314G>A | ||
| ENST00000578421.1:n.272+69G>A | ||
| ENST00000579286.5:n.245+69G>A | ||
| ENST00000579886.2:c.138+69G>A | ENSP00000463246.1:n.138+69G>A | |
| ENST00000580263.5:n.228+69G>A | ||
| ENST00000581562.5:n.185+69G>A | ||
| ENST00000582056.5:n.228+69G>A | ||
| ENST00000582356.5:n.263+69G>A | ||
| ENST00000583312.5:c.138+69G>A | ENSP00000467920.1:n.138+69G>A | |
| ENST00000584103.5:c.138+69G>A | ENSP00000465353.1:n.138+69G>A | |
| NM_000018.3:c.138+69G>A | NP_000009.1:n.138+69G>A | |
| NM_001033859.2:c.138+69G>A | NP_001029031.1:n.138+69G>A | |
| NM_001270447.1:c.207+69G>A | NP_001257376.1:n.207+69G>A | |
| NM_001270448.1:c.-91+69G>A | NP_001257377.1:n.-91+69G>A | |
| XM_006721516.2:c.138+69G>A | XP_006721579.2:n.138+69G>A | |
| XM_011523829.1:c.138+69G>A | XP_011522131.1:n.138+69G>A | |
| XM_011523830.1:c.138+69G>A | XP_011522132.1:n.138+69G>A | |
| XR_934021.1:n.245+69G>A | ||
| XR_934022.1:n.245+69G>A | ||
| XR_934023.1:n.245+69G>A | ||
| XM_006721516.3:c.138+69G>A | XP_006721579.2:n.138+69G>A | |
| XM_011523829.2:c.138+69G>A | XP_011522131.1:n.138+69G>A | |
| XM_011523830.2:c.138+69G>A | XP_011522132.1:n.138+69G>A | |
| XM_024450741.1:c.138+69G>A | XP_024306509.1:n.138+69G>A | |
| XR_934021.2:n.197+69G>A | ||
| XR_934022.2:n.197+69G>A | ||
| XR_934023.2:n.197+69G>A | ||
| NM_000018.4:c.138+69G>A MANE Select | NP_000009.1:n.138+69G>A | |
| NM_001033859.3:c.138+69G>A | NP_001029031.1:n.138+69G>A | |
| NM_001270447.2:c.207+69G>A | NP_001257376.1:n.207+69G>A | |
| NM_001270448.2:c.-91+69G>A | NP_001257377.1:n.-91+69G>A |