Linked Data
dbSNP Id:
rs1554292881
gnomAD v2:
7-41811798-C-CTTTTG
MyVariant Identifiers:
chr7:g.41811798_41811799insTTTTG (hg19)
chr7:g.41772200_41772201insTTTTG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.41772201_41772202insTTTGT , CM000669.2:g.41772201_41772202insTTTGT | GRCh38 |
| NC_000007.13:g.41811799_41811800insTTTGT , CM000669.1:g.41811799_41811800insTTTGT | GRCh37 |
| NC_000007.12:g.41778324_41778325insTTTGT | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_027118.1:n.359-695_359-694insTTTGT | ||
| NR_027118.2:n.356-695_356-694insTTTGT | ||
| XR_001745185.1:n.964+36487_964+36488insTTTGT | ||
| XR_001745186.1:n.954+36497_954+36498insTTTGT |