Canonical Allele Identifier: CA659015350
Gene:

Linked Data

dbSNP Id: rs1479037552

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101750664A>G , CM000672.2:g.101750664A>G GRCh38
NC_000010.10:g.103510421A>G , CM000672.1:g.103510421A>G GRCh37
NC_000010.9:g.103500411A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946255.1:n.217-6447T>C
XR_946255.2:n.217-6447T>C