Canonical Allele Identifier: CA1649534190
Gene:

Linked Data

dbSNP Id: rs1583228485

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98102315T>G , CM000668.2:g.98102315T>G GRCh38
NC_000006.11:g.98550191T>G , CM000668.1:g.98550191T>G GRCh37
NC_000006.10:g.98656912T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245563.2:n.456+3045T>G
XR_942809.1:n.456+3045T>G