Linked Data
ClinVar Variation Id:
2838563
ClinVar RCV Id:
RCV003652326
MyVariant Identifiers:
chr5:g.13770875C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.13770766C>T , CM000667.2:g.13770766C>T | GRCh38 |
| NC_000005.9:g.13770875C>T , CM000667.1:g.13770875C>T | GRCh37 |
| NC_000005.8:g.13823875C>T | NCBI36 |
| NG_013081.1:g.178715G>A | |
| NG_013081.2:g.178715G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265104.5:c.9588G>A MANE Select | ENSP00000265104.4:p.Val3196= | |
| ENST00000681290.1:c.9543G>A | ENSP00000505288.1:p.Val3181= | |
| ENST00000265104.4:c.9588G>A | ENSP00000265104.4:p.Val3196= | |
| ENST00000504001.3:n.300G>A | ||
| NM_001369.2:c.9588G>A | NP_001360.1:p.Val3196= | |
| XM_005248262.2:c.9543G>A | XP_005248319.1:p.Val3181= | |
| XM_005248262.3:c.9696G>A | XP_005248319.2:p.Val3232= | |
| XM_017009177.1:c.9696G>A | XP_016864666.1:p.Val3232= | |
| XM_017009178.1:c.8601G>A | XP_016864667.1:p.Val2867= | |
| XM_017009179.2:c.8601G>A | XP_016864668.1:p.Val2867= | |
| XM_017009180.1:c.9696G>A | XP_016864669.1:p.Val3232= | |
| XM_017009181.1:c.9696G>A | XP_016864670.1:p.Val3232= | |
| XM_017009182.1:c.9696G>A | XP_016864671.1:p.Val3232= | |
| XM_017009183.1:c.9696G>A | XP_016864672.1:p.Val3232= | |
| XM_017009185.1:c.4785G>A | XP_016864674.1:p.Val1595= | |
| XM_017009186.1:c.4338G>A | XP_016864675.1:p.Val1446= | |
| XM_017009188.1:c.3675G>A | XP_016864677.1:p.Val1225= | |
| XM_024454388.1:c.8601G>A | XP_024310156.1:p.Val2867= | |
| XM_024454389.1:c.8190G>A | XP_024310157.1:p.Val2730= | |
| NM_001369.3:c.9588G>A MANE Select | NP_001360.1:p.Val3196= |