Linked Data
ClinVar Variation Id:
2193037
ClinVar RCV Id:
RCV002607778
dbSNP Id:
rs776687942
gnomAD v2:
14-21161828-C-G
gnomAD v4:
14-20693669-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.20693669C>G , CM000676.2:g.20693669C>G | GRCh38 |
| NC_000014.8:g.21161828C>G , CM000676.1:g.21161828C>G | GRCh37 |
| NC_000014.7:g.20231668C>G | NCBI36 |
| NG_008717.2:g.14493C>G , LRG_653:g.14493C>G | |
| NG_033053.1:g.14457C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397990.5:c.105C>G (ANG) MANE Select | ENSP00000381077.4:p.Thr35= | |
| ENST00000555835.3:c.-17-5686C>G (RNASE4) MANE Select | ENSP00000452245.1:n.-17-5686C>G | |
| ENST00000336811.10:c.105C>G (ANG) | ENSP00000336762.6:p.Thr35= | |
| ENST00000397990.4:c.105C>G (ANG) | ENSP00000381077.4:p.Thr35= | |
| ENST00000397995.2:c.-17-5686C>G (RNASE4) | ENSP00000381081.2:n.-17-5686C>G | |
| ENST00000553909.1:c.86+19C>G | ENSP00000477037.1:n.86+19C>G | |
| ENST00000554073.1:n.146-5197C>G (ANG) | ||
| ENST00000555597.1:c.-18+4795C>G (RNASE4) | ENSP00000451624.1:n.-18+4795C>G | |
| ENST00000555835.2:c.-17-5686C>G (RNASE4) | ENSP00000452245.1:n.-17-5686C>G | |
| NM_001097577.2:c.105C>G (ANG) | NP_001091046.1:p.Thr35= | |
| NM_001145.4:c.105C>G , LRG_653t1:c.105C>G (ANG) | NP_001136.1:p.Thr35= | |
| NM_001282192.1:c.-18+19C>G (RNASE4) | NP_001269121.1:n.-18+19C>G | |
| NM_001282193.1:c.-17-5686C>G (RNASE4) | NP_001269122.1:n.-17-5686C>G | |
| NM_002937.4:c.-17-5686C>G (RNASE4) | NP_002928.1:n.-17-5686C>G | |
| NM_194431.2:c.-18+4795C>G (RNASE4) | NP_919412.1:n.-18+4795C>G | |
| NM_002937.5:c.-17-5686C>G (RNASE4) MANE Select | NP_002928.1:n.-17-5686C>G | |
| NM_001097577.3:c.105C>G (ANG) MANE Select | NP_001091046.1:p.Thr35= | |
| NM_001282192.2:c.-18+19C>G (RNASE4) | NP_001269121.1:n.-18+19C>G | |
| NM_001282193.2:c.-17-5686C>G (RNASE4) | NP_001269122.1:n.-17-5686C>G | |
| NM_194431.3:c.-18+4795C>G (RNASE4) | NP_919412.1:n.-18+4795C>G | |
| NM_001385271.1:c.105C>G (ANG) | NP_001372200.1:p.Thr35= | |
| NM_001385272.1:c.105C>G (ANG) | NP_001372201.1:p.Thr35= | |
| NM_001385273.1:c.105C>G (ANG) | NP_001372202.1:p.Thr35= | |
| NM_001385274.1:c.105C>G (ANG) | NP_001372203.1:p.Thr35= | |
| NR_174964.1:n.547G>C (EGILA) |