Linked Data
ClinVar Variation Id:
809932
ClinVar RCV Id:
RCV000998598
dbSNP Id:
rs1582780697
gnomAD v4:
6-42721948-G-A
MyVariant Identifiers:
chr6:g.42689686G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.42721948G>A , CM000668.2:g.42721948G>A | GRCh38 |
| NC_000006.11:g.42689686G>A , CM000668.1:g.42689686G>A | GRCh37 |
| NC_000006.10:g.42797664G>A | NCBI36 |
| NG_009176.1:g.5673C>T | |
| NG_009176.2:g.5673C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000230381.7:c.387C>T MANE Select | ENSP00000230381.5:p.Thr129= | |
| ENST00000230381.6:c.387C>T | ENSP00000230381.5:p.Thr129= | |
| NM_000322.4:c.387C>T | NP_000313.2:p.Thr129= | |
| XR_427834.2:n.1042C>T | ||
| XR_926295.1:n.1042C>T | ||
| XR_427834.4:n.1092C>T | ||
| XR_926295.3:n.1092C>T | ||
| NM_000322.5:c.387C>T MANE Select | NP_000313.2:p.Thr129= |