Linked Data
ClinVar Variation Id:
882865
ClinVar RCV Id:
RCV001112906
dbSNP Id:
rs200240901
ExAC:
14:21161761 T / C
gnomAD v2:
14-21161761-T-C
gnomAD v3:
14-20693602-T-C
gnomAD v4:
14-20693602-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.20693602T>C , CM000676.2:g.20693602T>C | GRCh38 |
| NC_000014.8:g.21161761T>C , CM000676.1:g.21161761T>C | GRCh37 |
| NC_000014.7:g.20231601T>C | NCBI36 |
| NG_008717.2:g.14426T>C , LRG_653:g.14426T>C | |
| NG_033053.1:g.14390T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397990.5:c.38T>C (ANG) MANE Select | ENSP00000381077.4:p.Val13Ala | |
| ENST00000555835.3:c.-17-5753T>C (RNASE4) MANE Select | ENSP00000452245.1:n.-17-5753T>C | |
| ENST00000336811.10:c.38T>C (ANG) | ENSP00000336762.6:p.Val13Ala | |
| ENST00000397990.4:c.38T>C (ANG) | ENSP00000381077.4:p.Val13Ala | |
| ENST00000397995.2:c.-17-5753T>C (RNASE4) | ENSP00000381081.2:n.-17-5753T>C | |
| ENST00000553909.1:c.38T>C | ENSP00000477037.1:p.Val13Ala | |
| ENST00000554073.1:n.146-5264T>C (ANG) | ||
| ENST00000555597.1:c.-18+4728T>C (RNASE4) | ENSP00000451624.1:n.-18+4728T>C | |
| ENST00000555835.2:c.-17-5753T>C (RNASE4) | ENSP00000452245.1:n.-17-5753T>C | |
| NM_001097577.2:c.38T>C (ANG) | NP_001091046.1:p.Val13Ala | |
| NM_001145.4:c.38T>C , LRG_653t1:c.38T>C (ANG) | NP_001136.1:p.Val13Ala | |
| NM_001282192.1:c.-66T>C (RNASE4) | NP_001269121.1:n.-66T>C | |
| NM_001282193.1:c.-17-5753T>C (RNASE4) | NP_001269122.1:n.-17-5753T>C | |
| NM_002937.4:c.-17-5753T>C (RNASE4) | NP_002928.1:n.-17-5753T>C | |
| NM_194431.2:c.-18+4728T>C (RNASE4) | NP_919412.1:n.-18+4728T>C | |
| NM_002937.5:c.-17-5753T>C (RNASE4) MANE Select | NP_002928.1:n.-17-5753T>C | |
| NM_001097577.3:c.38T>C (ANG) MANE Select | NP_001091046.1:p.Val13Ala | |
| NM_001282192.2:c.-66T>C (RNASE4) | NP_001269121.1:n.-66T>C | |
| NM_001282193.2:c.-17-5753T>C (RNASE4) | NP_001269122.1:n.-17-5753T>C | |
| NM_194431.3:c.-18+4728T>C (RNASE4) | NP_919412.1:n.-18+4728T>C | |
| NM_001385271.1:c.38T>C (ANG) | NP_001372200.1:p.Val13Ala | |
| NM_001385272.1:c.38T>C (ANG) | NP_001372201.1:p.Val13Ala | |
| NM_001385273.1:c.38T>C (ANG) | NP_001372202.1:p.Val13Ala | |
| NM_001385274.1:c.38T>C (ANG) | NP_001372203.1:p.Val13Ala | |
| NR_174964.1:n.614A>G (EGILA) |