Canonical Allele Identifier: CA1723810360
Gene:

Linked Data

dbSNP Id: rs1584380944

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87913747T>C , CM000669.2:g.87913747T>C GRCh38
NC_000007.13:g.87543062T>C , CM000669.1:g.87543062T>C GRCh37
NC_000007.12:g.87380998T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927723.1:n.148+154A>G
XR_927724.1:n.192+154A>G