Canonical Allele Identifier:
CA1500737785
Gene:
Linked Data
dbSNP Id:
rs1733826739
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.144559505A>G , CM000666.2:g.144559505A>G | GRCh38 |
| NC_000004.11:g.145480657A>G , CM000666.1:g.145480657A>G | GRCh37 |
| NC_000004.10:g.145700107A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649263.1:c.328-143527T>C | ENSP00000497507.1:n.328-143527T>C | |
| XR_939272.1:n.178+2479T>C | ||
| XR_939273.1:n.178+2479T>C | ||
| XR_939272.2:n.522+2479T>C | ||
| XR_939273.2:n.522+2479T>C |