Canonical Allele Identifier: CA2002397734
Gene:

Linked Data

dbSNP Id: rs2048667136

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116072514T>C , CM000673.2:g.116072514T>C GRCh38
NC_000011.9:g.115943232T>C , CM000673.1:g.115943232T>C GRCh37
NC_000011.8:g.115448442T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948055.1:n.192+500A>G
XR_948056.1:n.311-5309A>G
XR_948057.1:n.97+595A>G
XR_001748401.1:n.192+500A>G
XR_948055.2:n.192+500A>G
XR_948056.2:n.314-5309A>G
XR_948057.2:n.97+595A>G