Linked Data
ClinVar Variation Id:
161121
ClinVar RCV Id:
RCV001206535
dbSNP Id:
rs542652468
PubMed:
PMID:20301294
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.41986177G>T , CM000681.2:g.41986177G>T | GRCh38 |
| NC_000019.9:g.42490329G>T , CM000681.1:g.42490329G>T | GRCh37 |
| NC_000019.8:g.47182169G>T | NCBI36 |
| NG_008015.1:g.13054C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000545399.6:c.449C>A | ENSP00000444688.1:p.Ser150Tyr | |
| ENST00000644613.1:c.410C>A | ENSP00000494711.1:p.Ser137Tyr | |
| ENST00000645448.1:n.525C>A | ||
| ENST00000648268.1:c.410C>A MANE Select | ENSP00000498113.1:p.Ser137Tyr | |
| ENST00000302102.9:c.410C>A | ENSP00000302397.5:p.Ser137Tyr | |
| ENST00000441343.5:c.410C>A | ENSP00000411503.1:p.Ser137Tyr | |
| ENST00000473086.3:c.320C>A | ENSP00000469129.2:p.Ser107Tyr | |
| ENST00000543770.5:c.443C>A | ENSP00000437577.1:p.Ser148Tyr | |
| ENST00000545399.5:c.449C>A | ENSP00000444688.1:p.Ser150Tyr | |
| ENST00000602133.5:c.320C>A | ENSP00000471581.1:p.Ser107Tyr | |
| NM_001256213.1:c.443C>A | NP_001243142.1:p.Ser148Tyr | |
| NM_001256214.1:c.449C>A | NP_001243143.1:p.Ser150Tyr | |
| NM_152296.4:c.410C>A | NP_689509.1:p.Ser137Tyr | |
| XM_011526991.1:c.320C>A | XP_011525293.1:p.Ser107Tyr | |
| NM_152296.5:c.410C>A MANE Select | NP_689509.1:p.Ser137Tyr | |
| NM_001256214.2:c.449C>A | NP_001243143.1:p.Ser150Tyr | |
| NM_001256213.2:c.443C>A | NP_001243142.1:p.Ser148Tyr |