Linked Data
ClinVar Variation Id:
376489
ClinVar RCV Id:
RCV000417579
RCV000422347
RCV000421685
RCV000428271
RCV000428856
RCV000433058
RCV000438925
RCV000439528
RCV000438272
RCV000444032
RCV002051723
dbSNP Id:
rs1057519938
PubMed:
PMID:26619011
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.179203764A>C , CM000665.2:g.179203764A>C | GRCh38 |
| NC_000003.11:g.178921552A>C , CM000665.1:g.178921552A>C | GRCh37 |
| NC_000003.10:g.180404246A>C | NCBI36 |
| NG_012113.2:g.60242A>C , LRG_310:g.60242A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263967.4:c.1034A>C MANE Select | ENSP00000263967.3:p.Asn345Thr | |
| ENST00000643187.1:c.1034A>C | ENSP00000493507.1:p.Asn345Thr | |
| ENST00000674534.1:n.788A>C | ||
| ENST00000675467.1:n.3841A>C | ||
| ENST00000675786.1:c.1034A>C | ENSP00000502323.1:p.Asn345Thr | |
| ENST00000263967.3:c.1034A>C | ENSP00000263967.3:p.Asn345Thr | |
| NM_006218.2:c.1034A>C , LRG_310t1:c.1034A>C | NP_006209.2:p.Asn345Thr | |
| XM_006713658.2:c.1034A>C | XP_006713721.1:p.Asn345Thr | |
| XM_011512894.1:c.1034A>C | XP_011511196.1:p.Asn345Thr | |
| NM_006218.3:c.1034A>C | NP_006209.2:p.Asn345Thr | |
| XM_006713658.4:c.1034A>C | XP_006713721.1:p.Asn345Thr | |
| XM_011512894.2:c.1034A>C | XP_011511196.1:p.Asn345Thr | |
| NM_006218.4:c.1034A>C MANE Select | NP_006209.2:p.Asn345Thr |