Canonical Allele Identifier: CA1563552112
Gene:

Linked Data

dbSNP Id: rs1744564933

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.92222854T>C , CM000667.2:g.92222854T>C GRCh38
NC_000005.9:g.91518671T>C , CM000667.1:g.91518671T>C GRCh37
NC_000005.8:g.91554427T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948565.1:n.394+18170T>C