Canonical Allele Identifier:
CA440676025
Gene:
Linked Data
MyVariant Identifiers:
chr4:g.106463818G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.105542661G>A , CM000666.2:g.105542661G>A | GRCh38 |
| NC_000004.11:g.106463818G>A , CM000666.1:g.106463818G>A | GRCh37 |
| NC_000004.10:g.106683267G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_939038.1:n.344C>T | ||
| XR_939039.1:n.504C>T | ||
| XR_939040.1:n.296-1185C>T | ||
| XR_001741410.1:n.359C>T | ||
| XR_001741411.1:n.835C>T | ||
| XR_001741412.1:n.359C>T | ||
| XR_001741413.1:n.359C>T | ||
| XR_001741414.1:n.359C>T | ||
| XR_939038.2:n.359C>T | ||
| XR_939040.2:n.311-1185C>T |