Canonical Allele Identifier: CA93117912
Gene:

Linked Data

dbSNP Id: rs927043277

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578209dup , CM000666.2:g.12578209dup GRCh38
NC_000004.11:g.12579833dup , CM000666.1:g.12579833dup GRCh37
NC_000004.10:g.12188931dup NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31139dup
XR_001741374.1:n.254+44452dup
XR_925406.3:n.140+31139dup