Linked Data
dbSNP Id:
rs2095145639
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.5856994C>T , CM000680.2:g.5856994C>T | GRCh38 |
| NC_000018.9:g.5856993C>T , CM000680.1:g.5856993C>T | GRCh37 |
| NC_000018.8:g.5846993C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_172494.1:n.603-21449C>T | ||
| NR_172495.1:n.603-19259C>T | ||
| NR_172496.1:n.603-19259C>T | ||
| NR_172497.1:n.603-19259C>T | ||
| NR_172498.1:n.663-10119C>T | ||
| NR_172499.1:n.603-19259C>T | ||
| NR_172500.1:n.603-19259C>T | ||
| NR_172501.1:n.603-19259C>T | ||
| NR_172502.1:n.603-19259C>T | ||
| NR_172503.1:n.603-19259C>T |