Canonical Allele Identifier: CA1064182228
Gene:

Linked Data

dbSNP Id: rs1162853429

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.74553974dup , CM000666.2:g.74553974dup GRCh38
NC_000004.11:g.75419691dup , CM000666.1:g.75419691dup GRCh37
NC_000004.10:g.75638555dup NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001741513.1:n.167-1136dup