Linked Data
ClinVar Variation Id:
191207
dbSNP Id:
rs770045008
ExAC:
6:35471403 C / T
gnomAD v2:
6-35471403-C-T
gnomAD v3:
6-35503626-C-T
gnomAD v4:
6-35503626-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.35503626C>T , CM000668.2:g.35503626C>T | GRCh38 |
| NC_000006.11:g.35471403C>T , CM000668.1:g.35471403C>T | GRCh37 |
| NC_000006.10:g.35579381C>T | NCBI36 |
| NG_009077.1:g.14245G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000229771.11:c.1256G>A MANE Select | ENSP00000229771.6:p.Arg419Gln | |
| ENST00000229771.10:c.1256G>A | ENSP00000229771.6:p.Arg419Gln | |
| ENST00000322263.8:c.1097G>A | ENSP00000319414.4:p.Arg366Gln | |
| ENST00000495781.1:n.432G>A | ||
| ENST00000496434.5:n.273G>A | ||
| ENST00000614066.4:c.1250G>A | ENSP00000477534.1:p.Arg417Gln | |
| NM_001289395.1:c.1097G>A | NP_001276324.1:p.Arg366Gln | |
| NM_003322.4:c.1256G>A | NP_003313.3:p.Arg419Gln | |
| NM_003322.5:c.1256G>A | NP_003313.3:p.Arg419Gln | |
| NM_003322.6:c.1256G>A MANE Select | NP_003313.3:p.Arg419Gln | |
| NM_001289395.2:c.1097G>A | NP_001276324.1:p.Arg366Gln |