Linked Data
ClinVar Variation Id:
1979580
ClinVar RCV Id:
RCV002755970
dbSNP Id:
rs1749798972
gnomAD v3:
5-1278791-A-G
gnomAD v4:
5-1278791-A-G
MyVariant Identifiers:
chr5:g.1278906A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1278791A>G , CM000667.2:g.1278791A>G | GRCh38 |
| NC_000005.9:g.1278906A>G , CM000667.1:g.1278906A>G | GRCh37 |
| NC_000005.8:g.1331906A>G | NCBI36 |
| NG_009265.1:g.21257T>C , LRG_343:g.21257T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000310581.10:c.2136T>C MANE Select | ENSP00000309572.5:p.Asp712= | |
| ENST00000656021.1:c.*1682T>C | ENSP00000499759.1:n.*1682T>C | |
| ENST00000310581.9:c.2136T>C | ENSP00000309572.5:p.Asp712= | |
| ENST00000334602.10:c.2136T>C | ENSP00000334346.6:p.Asp712= | |
| ENST00000460137.6:c.2131-31T>C | ENSP00000425003.1:n.2131-31T>C | |
| ENST00000484238.6:n.949T>C | ||
| ENST00000508104.2:c.2136T>C | ENSP00000426042.2:p.Asp712= | |
| NM_001193376.1:c.2136T>C | NP_001180305.1:p.Asp712= | |
| NM_198253.2:c.2136T>C , LRG_343t1:c.2136T>C | NP_937983.2:p.Asp712= | |
| XM_011514104.1:c.606T>C | XP_011512406.1:p.Asp202= | |
| XM_011514105.1:c.492T>C | XP_011512407.1:p.Asp164= | |
| XM_011514106.1:c.492T>C | XP_011512408.1:p.Asp164= | |
| NR_149162.1:n.2194T>C | ||
| NR_149163.1:n.2189-31T>C | ||
| NM_001193376.2:c.2136T>C | NP_001180305.1:p.Asp712= | |
| NM_198253.3:c.2136T>C MANE Select | NP_937983.2:p.Asp712= | |
| NR_149162.2:n.2215T>C | ||
| NR_149163.2:n.2210-31T>C | ||
| NM_001193376.3:c.2136T>C | NP_001180305.1:p.Asp712= | |
| NR_149162.3:n.2215T>C | ||
| NR_149163.3:n.2210-31T>C |