Linked Data
dbSNP Id:
rs747427095
ExAC:
7:100230689 T / C
gnomAD v2:
7-100230689-T-C
gnomAD v3:
7-100633066-T-C
gnomAD v4:
7-100633066-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.100633066T>C , CM000669.2:g.100633066T>C | GRCh38 |
| NC_000007.13:g.100230689T>C , CM000669.1:g.100230689T>C | GRCh37 |
| NC_000007.12:g.100068625T>C | NCBI36 |
| NG_007989.1:g.13485A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000223051.8:c.784A>G MANE Select | ENSP00000223051.3:p.Arg262Gly | |
| ENST00000223051.7:c.784A>G | ENSP00000223051.3:p.Arg262Gly | |
| ENST00000431692.5:c.784A>G | ENSP00000413905.1:p.Arg262Gly | |
| ENST00000462090.5:n.25A>G | ||
| ENST00000462107.1:c.784A>G | ENSP00000420525.1:p.Arg262Gly | |
| ENST00000465294.5:n.789A>G | ||
| ENST00000473374.5:n.234A>G | ||
| ENST00000473571.1:n.238A>G | ||
| ENST00000475011.1:n.313A>G | ||
| ENST00000476304.5:n.405A>G | ||
| ENST00000490084.5:c.39A>G | ||
| NM_001206855.1:c.271A>G | NP_001193784.1:p.Arg91Gly | |
| NM_003227.3:c.784A>G | NP_003218.2:p.Arg262Gly | |
| XM_005250553.3:c.784A>G | XP_005250610.1:p.Arg262Gly | |
| XM_005250554.3:c.784A>G | XP_005250611.1:p.Arg262Gly | |
| NM_001206855.2:c.271A>G | NP_001193784.1:p.Arg91Gly | |
| XM_005250553.4:c.784A>G | XP_005250610.1:p.Arg262Gly | |
| XM_017012573.1:c.784A>G | XP_016868062.1:p.Arg262Gly | |
| NM_003227.4:c.784A>G MANE Select | NP_003218.2:p.Arg262Gly | |
| NM_001206855.3:c.271A>G | NP_001193784.1:p.Arg91Gly |