Canonical Allele Identifier: CA1769199343
Gene:

Linked Data

dbSNP Id: rs1021543166

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20130066G>C , CM000670.2:g.20130066G>C GRCh38
NC_000008.10:g.19987577G>C , CM000670.1:g.19987577G>C GRCh37
NC_000008.9:g.20031857G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949563.1:n.3408+147G>C
XR_949563.2:n.3400+147G>C