Canonical Allele Identifier: CA1649534228
Gene:

Linked Data

dbSNP Id: rs1773159143

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98102417dup , CM000668.2:g.98102417dup GRCh38
NC_000006.11:g.98550293dup , CM000668.1:g.98550293dup GRCh37
NC_000006.10:g.98657014dup NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245563.2:n.456+3147dup
XR_942809.1:n.456+3147dup