Canonical Allele Identifier:
CA440676048
Gene:
Linked Data
MyVariant Identifiers:
chr4:g.106463826A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.105542669A>T , CM000666.2:g.105542669A>T | GRCh38 |
| NC_000004.11:g.106463826A>T , CM000666.1:g.106463826A>T | GRCh37 |
| NC_000004.10:g.106683275A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_939038.1:n.336T>A | ||
| XR_939039.1:n.496T>A | ||
| XR_939040.1:n.296-1193T>A | ||
| XR_001741410.1:n.351T>A | ||
| XR_001741411.1:n.827T>A | ||
| XR_001741412.1:n.351T>A | ||
| XR_001741413.1:n.351T>A | ||
| XR_001741414.1:n.351T>A | ||
| XR_939038.2:n.351T>A | ||
| XR_939040.2:n.311-1193T>A |