Linked Data
ClinVar Variation Id:
895155
ClinVar RCV Id:
RCV001137080
dbSNP Id:
rs771800911
ExAC:
2:215843563 C / T
gnomAD v2:
2-215843563-C-T
gnomAD v3:
2-214978839-C-T
gnomAD v4:
2-214978839-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.214978839C>T , CM000664.2:g.214978839C>T | GRCh38 |
| NC_000002.11:g.215843563C>T , CM000664.1:g.215843563C>T | GRCh37 |
| NC_000002.10:g.215551808C>T | NCBI36 |
| NG_007074.1:g.164589G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272895.12:c.4942G>A MANE Select | ENSP00000272895.7:p.Gly1648Arg | |
| ENST00000272895.11:c.4942G>A | ENSP00000272895.7:p.Gly1648Arg | |
| ENST00000389661.4:c.3988G>A | ENSP00000374312.4:p.Gly1330Arg | |
| NM_015657.3:c.3988G>A | NP_056472.2:p.Gly1330Arg | |
| NM_173076.2:c.4942G>A | NP_775099.2:p.Gly1648Arg | |
| NR_103740.1:n.5242G>A | ||
| XM_011510951.1:c.4951G>A | XP_011509253.1:p.Gly1651Arg | |
| XM_011510952.1:c.4951G>A | XP_011509254.1:p.Gly1651Arg | |
| XM_011510951.2:c.4951G>A | XP_011509253.1:p.Gly1651Arg | |
| NM_173076.3:c.4942G>A MANE Select | NP_775099.2:p.Gly1648Arg | |
| NR_103740.2:n.5440G>A | ||
| NM_015657.4:c.3988G>A | NP_056472.2:p.Gly1330Arg |