Canonical Allele Identifier:
CA103381288
Gene:
Linked Data
dbSNP Id:
rs943392999
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.105542555A>C , CM000666.2:g.105542555A>C | GRCh38 |
| NC_000004.11:g.106463712A>C , CM000666.1:g.106463712A>C | GRCh37 |
| NC_000004.10:g.106683161A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_939038.1:n.450T>G | ||
| XR_939039.1:n.610T>G | ||
| XR_939040.1:n.296-1079T>G | ||
| XR_001741410.1:n.465T>G | ||
| XR_001741411.1:n.941T>G | ||
| XR_001741412.1:n.449+16T>G | ||
| XR_001741413.1:n.465T>G | ||
| XR_001741414.1:n.449+16T>G | ||
| XR_939038.2:n.465T>G | ||
| XR_939040.2:n.311-1079T>G |