Canonical Allele Identifier:
CA440676006
Gene:
Linked Data
MyVariant Identifiers:
chr4:g.106463811T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.105542654T>G , CM000666.2:g.105542654T>G | GRCh38 |
| NC_000004.11:g.106463811T>G , CM000666.1:g.106463811T>G | GRCh37 |
| NC_000004.10:g.106683260T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_939038.1:n.351A>C | ||
| XR_939039.1:n.511A>C | ||
| XR_939040.1:n.296-1178A>C | ||
| XR_001741410.1:n.366A>C | ||
| XR_001741411.1:n.842A>C | ||
| XR_001741412.1:n.366A>C | ||
| XR_001741413.1:n.366A>C | ||
| XR_001741414.1:n.366A>C | ||
| XR_939038.2:n.366A>C | ||
| XR_939040.2:n.311-1178A>C |