Linked Data
ClinVar Variation Id:
42865
ClinVar RCV Id:
RCV000035747
dbSNP Id:
rs397516121
gnomAD v4:
14-23427716-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23427716A>G , CM000676.2:g.23427716A>G | GRCh38 |
| NC_000014.8:g.23896925A>G , CM000676.1:g.23896925A>G | GRCh37 |
| NC_000014.7:g.22966765A>G | NCBI36 |
| NG_007884.1:g.12946T>C , LRG_384:g.12946T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000355349.4:c.1757T>C MANE Select | ENSP00000347507.3:p.Val586Ala | |
| ENST00000355349.3:c.1757T>C | ENSP00000347507.3:p.Val586Ala | |
| NM_000257.3:c.1757T>C | NP_000248.2:p.Val586Ala | |
| XR_245686.3:n.1863T>C | ||
| XM_017021340.1:c.1757T>C | XP_016876829.1:p.Val586Ala | |
| NM_000257.4:c.1757T>C MANE Select | NP_000248.2:p.Val586Ala |