Canonical Allele Identifier: CA1649534249
Gene:

Linked Data

dbSNP Id: rs1773160000

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98102452del , CM000668.2:g.98102452del GRCh38
NC_000006.11:g.98550328del , CM000668.1:g.98550328del GRCh37
NC_000006.10:g.98657049del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245563.2:n.456+3182del
XR_942809.1:n.456+3182del