Canonical Allele Identifier: CA1898741345
Gene:

Linked Data

dbSNP Id: rs4749388

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.29075776T>G , CM000672.2:g.29075776T>G GRCh38
NC_000010.10:g.29364705T>G , CM000672.1:g.29364705T>G GRCh37
NC_000010.9:g.29404711T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001747284.1:n.127-3716T>G