Canonical Allele Identifier: CA103381338
Gene:

Linked Data

dbSNP Id: rs1033354385
MyVariant Identifiers: chr4:g.106464118A>G (hg19) chr4:g.105542961A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542961A>G , CM000666.2:g.105542961A>G GRCh38
NC_000004.11:g.106464118A>G , CM000666.1:g.106464118A>G GRCh37
NC_000004.10:g.106683567A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.296-252T>C
XR_939039.1:n.456-252T>C
XR_939040.1:n.296-1485T>C
XR_001741410.1:n.311-252T>C
XR_001741411.1:n.787-252T>C
XR_001741412.1:n.311-252T>C
XR_001741413.1:n.311-252T>C
XR_001741414.1:n.311-252T>C
XR_939038.2:n.311-252T>C
XR_939040.2:n.311-1485T>C
Search 100 bp 5'
Search 100 bp 3'