Linked Data
dbSNP Id:
rs1733732571
gnomAD v3:
4-176666757-C-T
gnomAD v4:
4-176666757-C-T
COSMIC:
COSN6816122
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.176666757C>T , CM000666.2:g.176666757C>T | GRCh38 |
| NC_000004.11:g.177587908C>T , CM000666.1:g.177587908C>T | GRCh37 |
| NC_000004.10:g.177824902C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_939498.1:n.121-2864C>T | ||
| XR_939499.1:n.121-2864C>T | ||
| XR_939498.2:n.208-2864C>T | ||
| XR_939499.2:n.204-2864C>T |