Linked Data
ClinVar Variation Id:
351017
dbSNP Id:
rs776715085
ExAC:
5:13719094 G / A
gnomAD v2:
5-13719094-G-A
gnomAD v3:
5-13718985-G-A
gnomAD v4:
5-13718985-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.13718985G>A , CM000667.2:g.13718985G>A | GRCh38 |
| NC_000005.9:g.13719094G>A , CM000667.1:g.13719094G>A | GRCh37 |
| NC_000005.8:g.13772094G>A | NCBI36 |
| NG_013081.1:g.230496C>T | |
| NG_013081.2:g.230496C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265104.5:c.12396C>T MANE Select | ENSP00000265104.4:p.Thr4132= | |
| ENST00000681290.1:c.12351C>T | ENSP00000505288.1:p.Thr4117= | |
| ENST00000265104.4:c.12396C>T | ENSP00000265104.4:p.Thr4132= | |
| NM_001369.2:c.12396C>T | NP_001360.1:p.Thr4132= | |
| XM_005248262.2:c.12351C>T | XP_005248319.1:p.Thr4117= | |
| XM_005248262.3:c.12504C>T | XP_005248319.2:p.Thr4168= | |
| XM_017009177.1:c.12504C>T | XP_016864666.1:p.Thr4168= | |
| XM_017009178.1:c.11409C>T | XP_016864667.1:p.Thr3803= | |
| XM_017009179.2:c.11409C>T | XP_016864668.1:p.Thr3803= | |
| XM_017009180.1:c.12504C>T | XP_016864669.1:p.Thr4168= | |
| XM_017009185.1:c.7593C>T | XP_016864674.1:p.Thr2531= | |
| XM_017009186.1:c.7146C>T | XP_016864675.1:p.Thr2382= | |
| XM_017009188.1:c.6483C>T | XP_016864677.1:p.Thr2161= | |
| XM_024454388.1:c.11409C>T | XP_024310156.1:p.Thr3803= | |
| XM_024454389.1:c.10998C>T | XP_024310157.1:p.Thr3666= | |
| NM_001369.3:c.12396C>T MANE Select | NP_001360.1:p.Thr4132= |