Canonical Allele Identifier: CA1369169885
Gene:

Linked Data

dbSNP Id: rs1576348710

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.61428146G>A , CM000665.2:g.61428146G>A GRCh38
NC_000003.11:g.61413820G>A , CM000665.1:g.61413820G>A GRCh37
NC_000003.10:g.61388860G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940892.1:n.164+368C>T
XR_940893.1:n.164+368C>T
XR_001740725.1:n.202+368C>T
XR_940892.2:n.202+368C>T