Canonical Allele Identifier: CA1649498267
Gene:

Linked Data

dbSNP Id: rs1772157461

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98014713T>A , CM000668.2:g.98014713T>A GRCh38
NC_000006.11:g.98462589T>A , CM000668.1:g.98462589T>A GRCh37
NC_000006.10:g.98569310T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.371+45247T>A
XR_942809.1:n.371+45247T>A