Canonical Allele Identifier: CA1695966145
Gene:

Linked Data

dbSNP Id: rs1785080398

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.26605896A>G , CM000669.2:g.26605896A>G GRCh38
NC_000007.13:g.26645515A>G , CM000669.1:g.26645515A>G GRCh37
NC_000007.12:g.26612040A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927131.1:n.1118-6526T>C
XR_927131.2:n.1186-6526T>C