Canonical Allele Identifier:
CA440676002
Gene:
Linked Data
MyVariant Identifiers:
chr4:g.106463809C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.105542652C>G , CM000666.2:g.105542652C>G | GRCh38 |
| NC_000004.11:g.106463809C>G , CM000666.1:g.106463809C>G | GRCh37 |
| NC_000004.10:g.106683258C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_939038.1:n.353G>C | ||
| XR_939039.1:n.513G>C | ||
| XR_939040.1:n.296-1176G>C | ||
| XR_001741410.1:n.368G>C | ||
| XR_001741411.1:n.844G>C | ||
| XR_001741412.1:n.368G>C | ||
| XR_001741413.1:n.368G>C | ||
| XR_001741414.1:n.368G>C | ||
| XR_939038.2:n.368G>C | ||
| XR_939040.2:n.311-1176G>C |