Linked Data
ClinVar Variation Id:
2908097
ClinVar RCV Id:
RCV003606895
dbSNP Id:
rs753409781
ExAC:
17:42452040 C / T
gnomAD v2:
17-42452040-C-T
gnomAD v4:
17-44374672-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44374672C>T , CM000679.2:g.44374672C>T | GRCh38 |
| NC_000017.10:g.42452040C>T , CM000679.1:g.42452040C>T | GRCh37 |
| NC_000017.9:g.39807566C>T | NCBI36 |
| NG_008331.1:g.19834G>A , LRG_479:g.19834G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262407.6:c.2930G>A MANE Select | ENSP00000262407.5:p.Arg977Gln | |
| ENST00000648408.1:c.2361G>A | ||
| ENST00000262407.5:c.2930G>A | ENSP00000262407.5:p.Arg977Gln | |
| ENST00000587295.5:c.253+1161G>A | ||
| ENST00000588098.1:c.24G>A | ||
| ENST00000592462.5:n.2441G>A | ||
| NM_000419.3:c.2930G>A , LRG_479t1:c.2930G>A | NP_000410.2:p.Arg977Gln | |
| XM_011524749.1:c.2842-202G>A | XP_011523051.1:n.2842-202G>A | |
| XM_011524750.1:c.2930G>A | XP_011523052.1:p.Arg977Gln | |
| NM_000419.4:c.2930G>A | NP_000410.2:p.Arg977Gln | |
| NM_000419.5:c.2930G>A MANE Select | NP_000410.2:p.Arg977Gln |