Linked Data
ClinVar Variation Id:
750922
dbSNP Id:
rs1595081267
MyVariant Identifiers:
chr14:g.23892801G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23423592G>A , CM000676.2:g.23423592G>A | GRCh38 |
| NC_000014.8:g.23892801G>A , CM000676.1:g.23892801G>A | GRCh37 |
| NC_000014.7:g.22962641G>A | NCBI36 |
| NG_007884.1:g.17070C>T , LRG_384:g.17070C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355349.4:c.3054C>T MANE Select | ENSP00000347507.3:p.Asn1018= | |
| ENST00000355349.3:c.3054C>T | ENSP00000347507.3:p.Asn1018= | |
| NM_000257.3:c.3054C>T | NP_000248.2:p.Asn1018= | |
| XR_245686.3:n.3160C>T | ||
| XM_017021340.1:c.3054C>T | XP_016876829.1:p.Asn1018= | |
| NM_000257.4:c.3054C>T MANE Select | NP_000248.2:p.Asn1018= |