Canonical Allele Identifier:
CA440676018
Gene:
Linked Data
MyVariant Identifiers:
chr4:g.106463815C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.105542658C>T , CM000666.2:g.105542658C>T | GRCh38 |
| NC_000004.11:g.106463815C>T , CM000666.1:g.106463815C>T | GRCh37 |
| NC_000004.10:g.106683264C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_939038.1:n.347G>A | ||
| XR_939039.1:n.507G>A | ||
| XR_939040.1:n.296-1182G>A | ||
| XR_001741410.1:n.362G>A | ||
| XR_001741411.1:n.838G>A | ||
| XR_001741412.1:n.362G>A | ||
| XR_001741413.1:n.362G>A | ||
| XR_001741414.1:n.362G>A | ||
| XR_939038.2:n.362G>A | ||
| XR_939040.2:n.311-1182G>A |