Linked Data
ClinVar Variation Id:
2039510
ClinVar RCV Id:
RCV002907901
MyVariant Identifiers:
chr14:g.23884408G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23415199G>A , CM000676.2:g.23415199G>A | GRCh38 |
| NC_000014.8:g.23884408G>A , CM000676.1:g.23884408G>A | GRCh37 |
| NC_000014.7:g.22954248G>A | NCBI36 |
| NG_007884.1:g.25463C>T , LRG_384:g.25463C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355349.4:c.5355C>T MANE Select | ENSP00000347507.3:p.Asn1785= | |
| ENST00000355349.3:c.5355C>T | ENSP00000347507.3:p.Asn1785= | |
| NM_000257.3:c.5355C>T | NP_000248.2:p.Asn1785= | |
| XM_017021340.1:c.5355C>T | XP_016876829.1:p.Asn1785= | |
| NM_000257.4:c.5355C>T MANE Select | NP_000248.2:p.Asn1785= |