Canonical Allele Identifier:
CA440675948
Gene:
Linked Data
MyVariant Identifiers:
chr4:g.106463790G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.105542633G>T , CM000666.2:g.105542633G>T | GRCh38 |
| NC_000004.11:g.106463790G>T , CM000666.1:g.106463790G>T | GRCh37 |
| NC_000004.10:g.106683239G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_939038.1:n.372C>A | ||
| XR_939039.1:n.532C>A | ||
| XR_939040.1:n.296-1157C>A | ||
| XR_001741410.1:n.387C>A | ||
| XR_001741411.1:n.863C>A | ||
| XR_001741412.1:n.387C>A | ||
| XR_001741413.1:n.387C>A | ||
| XR_001741414.1:n.387C>A | ||
| XR_939038.2:n.387C>A | ||
| XR_939040.2:n.311-1157C>A |