Linked Data
ClinVar Variation Id:
1124123
ClinVar RCV Id:
RCV001455374
dbSNP Id:
rs2106427541
MyVariant Identifiers:
chr2:g.241808628G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240869211G>A , CM000664.2:g.240869211G>A | GRCh38 |
| NC_000002.11:g.241808628G>A , CM000664.1:g.241808628G>A | GRCh37 |
| NC_000002.10:g.241457301G>A | NCBI36 |
| NG_008005.1:g.5467G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307503.4:c.207G>A MANE Select | ENSP00000302620.3:p.Gln69= | |
| ENST00000307503.3:c.207G>A | ENSP00000302620.3:p.Gln69= | |
| ENST00000472436.1:n.227G>A | ||
| NM_000030.2:c.207G>A | NP_000021.1:p.Gln69= | |
| XR_924060.1:n.405+1022C>T | ||
| NM_000030.3:c.207G>A MANE Select | NP_000021.1:p.Gln69= |