Linked Data
ClinVar Variation Id:
2049533
ClinVar RCV Id:
RCV002914060
MyVariant Identifiers:
chr4:g.88533830T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.87612678T>C , CM000666.2:g.87612678T>C | GRCh38 |
| NC_000004.11:g.88533830T>C , CM000666.1:g.88533830T>C | GRCh37 |
| NC_000004.10:g.88752854T>C | NCBI36 |
| NG_011595.1:g.9150T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651931.1:c.492T>C MANE Select | ENSP00000498766.1:p.Asn164= | |
| ENST00000282478.7:c.492T>C | ENSP00000282478.7:p.Asn164= | |
| ENST00000399271.5:c.492T>C | ENSP00000382213.1:p.Asn164= | |
| NM_014208.3:c.492T>C MANE Select | NP_055023.2:p.Asn164= |