Canonical Allele Identifier: CA1932346145
Gene:

Linked Data

dbSNP Id: rs2064898860

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101750674A>C , CM000672.2:g.101750674A>C GRCh38
NC_000010.10:g.103510431A>C , CM000672.1:g.103510431A>C GRCh37
NC_000010.9:g.103500421A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_946255.1:n.217-6457T>G
XR_946255.2:n.217-6457T>G