Linked Data
dbSNP Id:
rs753337903
gnomAD v2:
2-31792522-G-GTATATATA
gnomAD v3:
2-31567452-G-GTATATATA
gnomAD v4:
2-31567452-G-GTATATATA
MyVariant Identifiers:
chr2:g.31792522_31792523insTATATATA (hg19)
chr2:g.31567452_31567453insTATATATA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.31567453_31567454insATATATAT , CM000664.2:g.31567453_31567454insATATATAT | GRCh38 |
| NC_000002.11:g.31792523_31792524insATATATAT , CM000664.1:g.31792523_31792524insATATATAT | GRCh37 |
| NC_000002.10:g.31646027_31646028insATATATAT | NCBI36 |
| NG_008365.1:g.18519_18520insTATATATA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000622030.2:c.281+13167_281+13168insTATATATA MANE Select | ENSP00000477587.1:n.281+13167_281+13168insTATATATA | |
| ENST00000622030.1:c.281+13167_281+13168insTATATATA | ENSP00000477587.1:n.281+13167_281+13168insTATATATA | |
| NM_000348.3:c.281+13167_281+13168insTATATATA | NP_000339.2:n.281+13167_281+13168insTATATATA | |
| XM_011533068.1:c.281+13167_281+13168insTATATATA | XP_011531370.1:n.281+13167_281+13168insTATATATA | |
| XM_011533070.1:c.27-33687_27-33686insTATATATA | XP_011531372.1:n.27-33687_27-33686insTATATATA | |
| XM_011533071.1:c.27-33687_27-33686insTATATATA | XP_011531373.1:n.27-33687_27-33686insTATATATA | |
| XM_011533072.1:c.27-33687_27-33686insTATATATA | XP_011531374.1:n.27-33687_27-33686insTATATATA | |
| XM_011533072.2:c.27-33687_27-33686insTATATATA | XP_011531374.1:n.27-33687_27-33686insTATATATA | |
| NM_000348.4:c.281+13167_281+13168insTATATATA MANE Select | NP_000339.2:n.281+13167_281+13168insTATATATA |