Canonical Allele Identifier: CA672122619
Gene:

Linked Data

dbSNP Id: rs894847855

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116072435C>G , CM000673.2:g.116072435C>G GRCh38
NC_000011.9:g.115943153C>G , CM000673.1:g.115943153C>G GRCh37
NC_000011.8:g.115448363C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948055.1:n.192+579G>C
XR_948056.1:n.311-5230G>C
XR_948057.1:n.97+674G>C
XR_001748401.1:n.192+579G>C
XR_948055.2:n.192+579G>C
XR_948056.2:n.314-5230G>C
XR_948057.2:n.97+674G>C