Canonical Allele Identifier: CA2731720111
Gene:

Linked Data

dbSNP Id: rs2141420799

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9249547G>C , CM000678.2:g.9249547G>C GRCh38
NC_000016.9:g.9343404G>C , CM000678.1:g.9343404G>C GRCh37
NC_000016.8:g.9250905G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933054.1:n.70+64814G>C