Linked Data
dbSNP Id:
rs2301364
gnomAD v2:
9-140034535-T-G
gnomAD v3:
9-137140083-T-G
gnomAD v4:
9-137140083-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.137140083T>G , CM000671.2:g.137140083T>G | GRCh38 |
| NC_000009.11:g.140034535T>G , CM000671.1:g.140034535T>G | GRCh37 |
| NC_000009.10:g.139154356T>G | NCBI36 |
| NG_011507.1:g.5927T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000371553.8:c.258+339T>G | ENSP00000360608.3:n.258+339T>G | |
| ENST00000371560.5:c.258+339T>G | ENSP00000360615.3:n.258+339T>G | |
| ENST00000371561.8:c.258+339T>G MANE Select | ENSP00000360616.3:n.258+339T>G | |
| ENST00000350902.9:c.258+339T>G | ENSP00000316915.9:n.258+339T>G | |
| ENST00000371546.8:c.258+339T>G | ENSP00000360601.4:n.258+339T>G | |
| ENST00000371550.8:c.258+339T>G | ENSP00000360605.4:n.258+339T>G | |
| ENST00000371553.7:c.258+339T>G | ENSP00000360608.3:n.258+339T>G | |
| ENST00000371555.8:c.258+339T>G | ENSP00000360610.4:n.258+339T>G | |
| ENST00000371559.8:c.258+339T>G | ENSP00000360614.4:n.258+339T>G | |
| ENST00000371560.4:c.258+339T>G | ENSP00000360615.3:n.258+339T>G | |
| ENST00000371561.7:c.258+339T>G | ENSP00000360616.3:n.258+339T>G | |
| ENST00000471122.5:n.335+339T>G | ||
| NM_000832.6:c.258+339T>G | NP_000823.4:n.258+339T>G | |
| NM_001185090.1:c.258+339T>G | NP_001172019.1:n.258+339T>G | |
| NM_001185091.1:c.258+339T>G | NP_001172020.1:n.258+339T>G | |
| NM_007327.3:c.258+339T>G | NP_015566.1:n.258+339T>G | |
| NM_021569.3:c.258+339T>G | NP_067544.1:n.258+339T>G | |
| XM_005266071.2:c.258+339T>G | XP_005266128.1:n.258+339T>G | |
| XM_005266072.2:c.258+339T>G | XP_005266129.1:n.258+339T>G | |
| XM_005266073.3:c.258+339T>G | XP_005266130.1:n.258+339T>G | |
| XM_011518583.1:c.258+339T>G | XP_011516885.1:n.258+339T>G | |
| XM_005266071.3:c.258+339T>G | XP_005266128.1:n.258+339T>G | |
| XM_005266072.3:c.258+339T>G | XP_005266129.1:n.258+339T>G | |
| XM_005266073.4:c.258+339T>G | XP_005266130.1:n.258+339T>G | |
| XM_011518583.2:c.258+339T>G | XP_011516885.1:n.258+339T>G | |
| NM_007327.4:c.258+339T>G MANE Select | NP_015566.1:n.258+339T>G | |
| NM_000832.7:c.258+339T>G | NP_000823.4:n.258+339T>G | |
| NM_001185090.2:c.258+339T>G | NP_001172019.1:n.258+339T>G | |
| NM_001185091.2:c.258+339T>G | NP_001172020.1:n.258+339T>G | |
| NM_021569.4:c.258+339T>G | NP_067544.1:n.258+339T>G |