Canonical Allele Identifier: CA1889449163
Gene:

Linked Data

dbSNP Id: rs2797288

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.9011210G>C , CM000672.2:g.9011210G>C GRCh38
NC_000010.10:g.9053173G>C , CM000672.1:g.9053173G>C GRCh37
NC_000010.9:g.9093179G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930641.1:n.32+54153C>G