Canonical Allele Identifier:
CA440676012
Gene:
Linked Data
MyVariant Identifiers:
chr4:g.106463813T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.105542656T>G , CM000666.2:g.105542656T>G | GRCh38 |
| NC_000004.11:g.106463813T>G , CM000666.1:g.106463813T>G | GRCh37 |
| NC_000004.10:g.106683262T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_939038.1:n.349A>C | ||
| XR_939039.1:n.509A>C | ||
| XR_939040.1:n.296-1180A>C | ||
| XR_001741410.1:n.364A>C | ||
| XR_001741411.1:n.840A>C | ||
| XR_001741412.1:n.364A>C | ||
| XR_001741413.1:n.364A>C | ||
| XR_001741414.1:n.364A>C | ||
| XR_939038.2:n.364A>C | ||
| XR_939040.2:n.311-1180A>C |