Linked Data
MyVariant Identifiers:
chr11:g.46749705C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.46728155C>A , CM000673.2:g.46728155C>A | GRCh38 |
| NC_000011.9:g.46749705C>A , CM000673.1:g.46749705C>A | GRCh37 |
| NC_000011.8:g.46706281C>A | NCBI36 |
| NG_008953.1:g.13963C>A , LRG_551:g.13963C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311907.10:c.1290C>A MANE Select | ENSP00000308541.5:p.Ser430= | |
| ENST00000311907.9:c.1290C>A | ENSP00000308541.5:p.Ser430= | |
| ENST00000530231.5:c.1290C>A | ENSP00000433907.1:p.Ser430= | |
| NM_000506.3:c.1290C>A | NP_000497.1:p.Ser430= | |
| NM_000506.4:c.1290C>A , LRG_551t1:c.1290C>A | NP_000497.1:p.Ser430= | |
| NM_001311257.1:c.1242C>A | NP_001298186.1:p.Ser414= | |
| XR_428840.2:n.1334C>A | ||
| XR_428840.4:n.1325C>A | ||
| NM_000506.5:c.1290C>A MANE Select | NP_000497.1:p.Ser430= | |
| NM_001311257.2:c.1242C>A | NP_001298186.1:p.Ser414= |