Linked Data
ClinVar Variation Id:
2009707
ClinVar RCV Id:
RCV002842631
gnomAD v4:
5-13770952-A-G
MyVariant Identifiers:
chr5:g.13771061A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.13770952A>G , CM000667.2:g.13770952A>G | GRCh38 |
| NC_000005.9:g.13771061A>G , CM000667.1:g.13771061A>G | GRCh37 |
| NC_000005.8:g.13824061A>G | NCBI36 |
| NG_013081.1:g.178529T>C | |
| NG_013081.2:g.178529T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265104.5:c.9402T>C MANE Select | ENSP00000265104.4:p.Asp3134= | |
| ENST00000681290.1:c.9357T>C | ENSP00000505288.1:p.Asp3119= | |
| ENST00000265104.4:c.9402T>C | ENSP00000265104.4:p.Asp3134= | |
| ENST00000504001.3:n.114T>C | ||
| NM_001369.2:c.9402T>C | NP_001360.1:p.Asp3134= | |
| XM_005248262.2:c.9357T>C | XP_005248319.1:p.Asp3119= | |
| XM_005248262.3:c.9510T>C | XP_005248319.2:p.Asp3170= | |
| XM_017009177.1:c.9510T>C | XP_016864666.1:p.Asp3170= | |
| XM_017009178.1:c.8415T>C | XP_016864667.1:p.Asp2805= | |
| XM_017009179.2:c.8415T>C | XP_016864668.1:p.Asp2805= | |
| XM_017009180.1:c.9510T>C | XP_016864669.1:p.Asp3170= | |
| XM_017009181.1:c.9510T>C | XP_016864670.1:p.Asp3170= | |
| XM_017009182.1:c.9510T>C | XP_016864671.1:p.Asp3170= | |
| XM_017009183.1:c.9510T>C | XP_016864672.1:p.Asp3170= | |
| XM_017009185.1:c.4599T>C | XP_016864674.1:p.Asp1533= | |
| XM_017009186.1:c.4152T>C | XP_016864675.1:p.Asp1384= | |
| XM_017009188.1:c.3489T>C | XP_016864677.1:p.Asp1163= | |
| XM_024454388.1:c.8415T>C | XP_024310156.1:p.Asp2805= | |
| XM_024454389.1:c.8004T>C | XP_024310157.1:p.Asp2668= | |
| NM_001369.3:c.9402T>C MANE Select | NP_001360.1:p.Asp3134= |