Canonical Allele Identifier:
CA440675791
Gene:
Linked Data
MyVariant Identifiers:
chr4:g.106463736G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.105542579G>T , CM000666.2:g.105542579G>T | GRCh38 |
| NC_000004.11:g.106463736G>T , CM000666.1:g.106463736G>T | GRCh37 |
| NC_000004.10:g.106683185G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_939038.1:n.426C>A | ||
| XR_939039.1:n.586C>A | ||
| XR_939040.1:n.296-1103C>A | ||
| XR_001741410.1:n.441C>A | ||
| XR_001741411.1:n.917C>A | ||
| XR_001741412.1:n.441C>A | ||
| XR_001741413.1:n.441C>A | ||
| XR_001741414.1:n.441C>A | ||
| XR_939038.2:n.441C>A | ||
| XR_939040.2:n.311-1103C>A |