Canonical Allele Identifier: CA1369169911
Gene:

Linked Data

dbSNP Id: rs2041753638

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.61428207G>A , CM000665.2:g.61428207G>A GRCh38
NC_000003.11:g.61413881G>A , CM000665.1:g.61413881G>A GRCh37
NC_000003.10:g.61388921G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940892.1:n.164+307C>T
XR_940893.1:n.164+307C>T
XR_001740725.1:n.202+307C>T
XR_940892.2:n.202+307C>T