Linked Data
dbSNP Id:
rs1557069293
gnomAD v2:
X-76829911-T-C
gnomAD v3:
X-77574446-T-C
gnomAD v4:
X-77574446-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.77574446T>C , CM000685.2:g.77574446T>C | GRCh38 |
| NC_000023.10:g.76829911T>C , CM000685.1:g.76829911T>C | GRCh37 |
| NC_000023.9:g.76716567T>C | NCBI36 |
| NG_008838.2:g.216776A>G | |
| NG_008838.3:g.216824A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373344.11:c.6218-88A>G MANE Select | ENSP00000362441.4:n.6218-88A>G | |
| ENST00000636152.1:n.53-88A>G | ||
| ENST00000675732.1:c.1316-88A>G | ENSP00000502598.1:n.1316-88A>G | |
| ENST00000373344.9:c.6218-88A>G | ENSP00000362441.4:n.6218-88A>G | |
| ENST00000395603.7:c.6104-88A>G | ENSP00000378967.3:n.6104-88A>G | |
| ENST00000480283.5:c.*5846-88A>G | ENSP00000480196.1:n.*5846-88A>G | |
| ENST00000623316.1:c.702-88A>G | ||
| ENST00000623706.3:n.3288-88A>G | ||
| NM_000489.4:c.6218-88A>G | NP_000480.3:n.6218-88A>G | |
| NM_138270.3:c.6104-88A>G | NP_612114.2:n.6104-88A>G | |
| XM_005262153.3:c.6215-88A>G | XP_005262210.2:n.6215-88A>G | |
| XM_005262154.3:c.6131-88A>G | XP_005262211.2:n.6131-88A>G | |
| XM_005262155.3:c.6101-88A>G | XP_005262212.2:n.6101-88A>G | |
| XM_005262156.3:c.6053-88A>G | XP_005262213.2:n.6053-88A>G | |
| XM_005262157.3:c.6014-88A>G | XP_005262214.2:n.6014-88A>G | |
| XM_006724666.2:c.6101-88A>G | XP_006724729.1:n.6101-88A>G | |
| XM_006724667.2:c.5939-88A>G | XP_006724730.1:n.5939-88A>G | |
| XR_938400.1:n.6560-88A>G | ||
| NM_000489.5:c.6218-88A>G | NP_000480.3:n.6218-88A>G | |
| XM_005262153.5:c.6215-88A>G | XP_005262210.2:n.6215-88A>G | |
| XM_005262154.5:c.6131-88A>G | XP_005262211.2:n.6131-88A>G | |
| XM_005262155.4:c.6101-88A>G | XP_005262212.2:n.6101-88A>G | |
| XM_005262156.4:c.6053-88A>G | XP_005262213.2:n.6053-88A>G | |
| XM_005262157.5:c.6014-88A>G | XP_005262214.2:n.6014-88A>G | |
| XM_006724666.4:c.6101-88A>G | XP_006724729.1:n.6101-88A>G | |
| XM_006724667.3:c.5939-88A>G | XP_006724730.1:n.5939-88A>G | |
| XM_017029601.2:c.6128-88A>G | XP_016885090.1:n.6128-88A>G | |
| XM_017029602.1:c.6098-88A>G | XP_016885091.1:n.6098-88A>G | |
| XM_017029603.1:c.6050-88A>G | XP_016885092.1:n.6050-88A>G | |
| XM_017029604.2:c.6017-88A>G | XP_016885093.1:n.6017-88A>G | |
| XM_017029605.1:c.6014-88A>G | XP_016885094.1:n.6014-88A>G | |
| XM_017029606.2:c.5987-88A>G | XP_016885095.1:n.5987-88A>G | |
| XM_017029607.2:c.5984-88A>G | XP_016885096.1:n.5984-88A>G | |
| XM_017029608.2:c.5936-88A>G | XP_016885097.1:n.5936-88A>G | |
| XM_017029609.1:c.5900-88A>G | XP_016885098.1:n.5900-88A>G | |
| XM_017029610.1:c.5897-88A>G | XP_016885099.1:n.5897-88A>G | |
| XM_017029611.1:c.5852-88A>G | XP_016885100.1:n.5852-88A>G | |
| XR_001755700.2:n.6517-88A>G | ||
| NM_138270.4:c.6104-88A>G | NP_612114.2:n.6104-88A>G | |
| NM_000489.6:c.6218-88A>G MANE Select | NP_000480.3:n.6218-88A>G | |
| NM_138270.5:c.6104-88A>G | NP_612114.2:n.6104-88A>G |