Canonical Allele Identifier: CA106421597
Gene:

Linked Data

dbSNP Id: rs937296920
MyVariant Identifiers: chr4:g.134601486G>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601486G>T , CM000666.2:g.134601486G>T GRCh38
NC_000004.11:g.135522641G>T , CM000666.1:g.135522641G>T GRCh37
NC_000004.10:g.135742091G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939212.1:n.410+14127G>T
XR_939214.1:n.392+14127G>T
XR_939214.2:n.392+14127G>T